Product Recall Checker | Search Product Recalls by UPC, Lot Code, Brand or Model

Latest Product Recall Matches

Showing 851 - 875 of 4,975 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Reign Medical Clench Staple System (Compression), Description/REF: 9mm x 7mm/152-30907; 11mm x 10mm/152-31110; 15mm x 12mm/152-31512; 18mm x 18mm/152-31818; 20mm x 20mm/152-32020; 9mm x 7mm/152-40907; 11mm x 10mm/152-41110; 15mm x 12mm/152-41512; 18mm x 18mm/152-41818; 20mm x 20mm/152-42020 Bone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established.	FDA Z-3211-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 15, 2026	Details
SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components manufactured from UHMWPE (polyethylene) Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.	FDA Z-3206-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 30, 2026	Details
Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death.	FDA Z-3121-2026	Medical Device	High	Sep 23, 2026 Recall: Aug 11, 2026	Details
Philips PIC iX Essentials REF:867093 Due to software malfunction, patient information system may freeze and become unresponsive.	FDA Z-3142-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 31, 2026	Details
IV Sets with drip chambers Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.	FDA Z-3161-2026	Medical Device	High	Sep 23, 2026 Recall: May 12, 2026	Details
Plum administration sets Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.	FDA Z-3156-2026	Medical Device	High	Sep 23, 2026 Recall: May 12, 2026	Details
StatStrip Glucose Hospital Meter System. Model No: 63685. Glucose test system. A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also affects QC barcode scanning: if a QC scan triggers the same retention behavior, QC results may be attributed to an incorrect identifier or QC tests may fail without the user recognizing the underlying cause. This defect does not affect the analytical accuracy of glucose measurements.	FDA Z-3128-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 29, 2026	Details
StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system. A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also affects QC barcode scanning: if a QC scan triggers the same retention behavior, QC results may be attributed to an incorrect identifier or QC tests may fail without the user recognizing the underlying cause. This defect does not affect the analytical accuracy of glucose measurements.	FDA Z-3130-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 29, 2026	Details
Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03; Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.	FDA Z-3154-2026	Medical Device	High	Sep 23, 2026 Recall: Aug 10, 2026	Details
Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, IN; Product Code: 0042-0000-IN. 4. Impella Controller, Packaged, JP; Product Code: 0042-0000-JP. 5. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK. 6. Impella Controller, Packaged, US; Product Code: 0042-0000-US. The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.	FDA Z-3148-2026	Medical Device	High	Sep 23, 2026 Recall: Aug 12, 2026	Details
Centricity PACS Server V7, intended for managing digital medical images and associated data, All versions Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.	FDA Z-3169-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 31, 2026	Details
Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101 S2107-110 Extra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA.	FDA Z-3175-2026	Medical Device	High	Sep 23, 2026 Recall: Aug 7, 2026	Details
IV Sets with drip chambers Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.	FDA Z-3160-2026	Medical Device	High	Sep 23, 2026 Recall: May 12, 2026	Details
Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N The kits contain a Retrograde Coronary Sinus Perfusion (RCSP) cannulae that has the potential for a sterile barrier breach. Sterility of the product cannot be assured. If a compromised pouch seal is not identified prior to use and the cannula is used, there is a potential risk of infection or other complications associated with the use of a non-sterile device, including hemolysis, foreign body reaction, thromboembolism, and/or organ dysfunction.	FDA Z-3137-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 23, 2026	Details
Oncology sets with drip chambers Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.	FDA Z-3158-2026	Medical Device	High	Sep 23, 2026 Recall: May 12, 2026	Details
Aisys CS2, Datex-Ohmeda anesthesia system, Part Number 1011-9055-000 Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarms. When this issue occurs, anesthetic agent delivery will be interrupted and requires clinician intervention. If this is not provided, the patient may experience decreased anesthetic agent effect.	FDA Z-3190-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 30, 2026	Details
Oncology sets with drip chambers Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.	FDA Z-3159-2026	Medical Device	High	Sep 23, 2026 Recall: May 12, 2026	Details
StatStrip Glucose and B- Ketone meter. Model No: 63910. Glucose test system. A software synchronization/timing issue in the barcode scanning and patient data processing component that causes the device to intermittently retain a previously scanned barcode including patient identification (ID) barcodes and quality control (QC) solution ID barcodes when a new barcode is scanned, resulting in the prior barcode information remaining displayed on the screen for the current test. When this defect occurs and the operator accepts the incorrectly displayed patient information without recognizing the mismatch, the current patient's glucose result will be incorrectly assigned to the previous patient's medical record and transmitted to the data management system (DMS), and the current patient's medical record will not receive a result, leaving their glucose status unrecorded and their clinical management without the information needed to guide treatment decisions. The previous patient, whose medical record now contains a glucose result that does not belong to them, may receive inappropriate clinical intervention based on that erroneous result, particularly in critically ill patients, neonates, and infants who cannot communicate symptoms or self-treat. The defect also affects QC barcode scanning: if a QC scan triggers the same retention behavior, QC results may be attributed to an incorrect identifier or QC tests may fail without the user recognizing the underlying cause. This defect does not affect the analytical accuracy of glucose measurements.	FDA Z-3131-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 29, 2026	Details
Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code STU CSCS V3 MAI800 Integrated Part Number 5867474-03 Product Code STV Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.	FDA Z-3143-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 30, 2026	Details
Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: DYKM2187A The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death.	FDA Z-3125-2026	Medical Device	High	Sep 23, 2026 Recall: Aug 11, 2026	Details
Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02; Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.	FDA Z-3151-2026	Medical Device	High	Sep 23, 2026 Recall: Aug 10, 2026	Details
Et Control, Software option for anesthesia gas machine to achieve and maintain targeted end tidal oxygen and anesthetic agents, Field replaceable unit (FRU) part numbers: 1011-8000-000-S, 5700665 Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarms. When this issue occurs, anesthetic agent delivery will be interrupted and requires clinician intervention. If this is not provided, the patient may experience decreased anesthetic agent effect.	FDA Z-3192-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 30, 2026	Details
Aisys CS2 with Et Control, Datex-Ohmeda anesthesia system, Part Number 1011-9000-000 Anesthesia Delivery Systems containing certain electronic gas mixer assemblies can automatically transition to Alternate O2 control. In Alternate O2 control, the system delivers 100% O2 to the breathing system enabling continued controlled or manual ventilation and initiates audible and visual alarms. When this issue occurs, anesthetic agent delivery will be interrupted and requires clinician intervention. If this is not provided, the patient may experience decreased anesthetic agent effect.	FDA Z-3191-2026	Medical Device	High	Sep 23, 2026 Recall: Jul 30, 2026	Details
REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM Reusable access port system may crack or seperate during use.	FDA Z-3183-2026	Medical Device	High	Sep 23, 2026 Recall: Aug 19, 2026	Details
Powertrain Control Module May Cause a Loss of Drive Power Jaguar Land Rover North America, LLC (Land Rover) is recalling one 2026 Range Rover Sport vehicle. The circuit board in the powertrain control module (PCM) was misaligned during production and may be deformed. A deformed circuit board may cause a loss of drive power, increases the risk of a crash.	NHTSA 26V607000	Vehicle	High	Sep 23, 2026 Recall: Sep 23, 2026	Details

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What To Enter In The Search Box

A recall usually applies to specific products, batches, model ranges or dates. Use the details printed on the item, package, label, receipt or vehicle paperwork.

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VIN Or NHTSA Campaign

This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.

Official Sources This Checker Organizes

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CPSC

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Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.

How To Confirm A Recall Match

1. Search The Obvious Name First

Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.

2. Open The Closest Result

Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.

3. Match Every Identifier

Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.

4. Follow The Official Remedy

The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.

When A Recall Result Looks Like Your Product

Use this checklist before you throw away a product, call the company, request a refund or schedule a repair.

If It Is Food, Formula Or Pet Food

Do not rely on brand alone. Match the package size, UPC, lot code, best-by date, use-by date, distribution states and any allergy or contamination warning.

If It Is A Baby Or Household Product

Look for model number, date code, serial range, color, size, online listing, product photo and the exact hazard such as choking, suffocation, fire or fall risk.

If It Is A Vehicle Or Car Seat

Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.

If The Details Do Not Match

Your item may not be part of that specific recall. Check spelling, older notices, retailer alerts and the official source before deciding it is safe.

What Is A Product Recall?

A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.

What Should You Do After Finding A Recall?

If all affected details match, follow the official instructions. Keep packaging, take photos, save receipts and contact the company or retailer when a refund or repair is offered.

Why Recall Details Must Match Exactly

A similar brand or product name is not enough. UPCs, lot codes, dates, model numbers, serial ranges and distribution areas determine whether your item is included.

How To Avoid Fake Recall Notices

Be careful with text messages, social posts or refund forms that ask for private information. Verify the notice through an official agency, retailer or manufacturer page.

Product Recall FAQ

Short answers for common product recall searches.

Can I search product recalls by UPC code?

Yes, when the official recall notice includes a UPC or product code. If no result appears, also search the brand, product name, package size, lot code and company name.

Can I search product recalls by lot code?

Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.

Does this replace a VIN recall lookup?

No. This tool helps find vehicle recall campaigns and NHTSA numbers. Use the official NHTSA VIN or license plate lookup for vehicle-specific unrepaired recall status.

Are all recalls listed here?

The database combines multiple official U.S. sources, but agencies and companies can publish or update notices at different times. Always check the linked official notice before taking final action.

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