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

Latest Product Recall Matches

Showing 151 - 175 of 3,083 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.	FDA Z-2649-2026	Medical Device	High	Jul 8, 2026 Recall: Jun 1, 2026	Details
Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART DYNJ909090B OPEN HEART CDS QVH CDS982523M Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.	FDA Z-2611-2026	Medical Device	High	Jul 8, 2026 Recall: May 28, 2026	Details
Medline Convenience Kits: 1) IMAGING BIOPSY TRAY, Model Number: DYNDH1068; 2) BREAST BIOPSY PACK, Model Number: PHS234706I The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.	FDA Z-2539-2026	Medical Device	High	Jul 8, 2026 Recall: May 21, 2026	Details
Medline Convenience Kits: 1) STD, INTRO-FLEX INTRODUCER 6F, C, Model Number: I550BF6C; 2) STD, INTRO-FLEX INTRODUCER 9F, C, Model Number: I505BF9C The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.	FDA Z-2538-2026	Medical Device	High	Jul 8, 2026 Recall: May 21, 2026	Details
5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107177 5855300 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107184 5865120 Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107191 5865200 Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI_DI Code: 00801741107214 5865240 Power-Trialysis Slim-Cath Precurved Extension Short-Term Dialysis Catheter 12 Fr Triple-Lumen Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.	FDA Z-2661-2026	Medical Device	High	Jul 8, 2026 Recall: May 21, 2026	Details
Radius VSM ECG pre-connected Set, REF: 4842, 4695 Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.	FDA Z-2670-2026	Medical Device	High	Jul 8, 2026 Recall: Feb 20, 2026	Details
Medline Convenience Kits: 1) SUTURE TRAY, Model Number: SUT12260; 2) CHEST TUBE INSERTION TRAY, Model Number: MNS3390; 3) CONTRACEPTIVE IMPLANT INSERTION KIT, Model Number: MNS9715; 4) 20GX3" RADIAL ART LINE KIT, Model Number: ART351; 5) MYELOGRAM PACK, Model Number: P155615A; 6) CHEST TUBE INSERTION TRAY, Model Number: MNS3390; 7) LACERATION TRAY, Model Number: SUT18660A; 8) GENERAL BIOPSY TRAY, Model Number: MNS5985; 9) LACERATION TRAY, Model Number: DYNDL1351; 10) 20GX3" RADIAL ART LINE KIT, Model Number: ART351; 11) ARTERIAL LINE TRAY, Model Number: ART600; 12) SUTURE TRAY, Model Number: S The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.	FDA Z-2542-2026	Medical Device	High	Jul 8, 2026 Recall: May 21, 2026	Details
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105 200106 200108 200110 200112 200120 200121 200123 200131 Software Version: N/A Product Description: Wecksorb Neurosponges are made of an absorbent cotton material. Certain Neurosponge varieties are available with an x-ray detectable thread to assist with location within the surgical site. Some Neurosponges (patties) have a string for accountability during the post-surgical verification process. Wecksorb Ne Due to out-of-specification, or potential out-of-specification, levels of endotoxins	FDA Z-2639-2026	Medical Device	High	Jul 8, 2026 Recall: May 7, 2026	Details
CRE Pro Wireguided 12-15mm 240cm Potential sterile breach of the pouches in which devices are packaged.	FDA Z-2629-2026	Medical Device	High	Jul 8, 2026 Recall: May 21, 2026	Details
Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ901328G HEART A DYNJ903465K OPEN HEART DYNJ909090G SILVER CROSS OPEN HEART DYNJ906102M VPH OPEN HEART DYNJ902664M DYNJ902664N Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.	FDA Z-2607-2026	Medical Device	High	Jul 8, 2026 Recall: May 28, 2026	Details
CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 The Poly Per-Q-Cath Midline catheters are indicated for short or long term peripheral access to the peripheral venous system for selected intravenous therapies and blood sarnpling. Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.	FDA Z-2656-2026	Medical Device	High	Jul 8, 2026 Recall: May 21, 2026	Details
RayCare 2024A SP1. Oncology Information Systems. Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.	FDA Z-2646-2026	Medical Device	High	Jul 8, 2026 Recall: May 20, 2026	Details
Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG PACK DYNJ905857 OH MED RN CDS DYNJ905936B Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.	FDA Z-2609-2026	Medical Device	High	Jul 8, 2026 Recall: May 28, 2026	Details
GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460 Reduced or no recovery of some strains of Neisseria gonorrhoeae.	FDA Z-2623-2026	Medical Device	High	Jul 8, 2026 Recall: Jun 3, 2026	Details
Incorrect Weight Rating on Label/FMVSS 110 Subaru of America, Inc. (Subaru) is recalling certain 2026 Crosstrek Hybrid, 2025-2026 Forester Hybrid, Forester, and 2019-2026 Ascent vehicles. These vehicles were manufactured with an incorrect Gross Axle Weight Rating (GAWR) on the certification label. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) 110, "Tire selection and rims." An incorrect GAWR label may lead to an overloaded vehicle, increasing the risk of a crash.	NHTSA 26V436000	Vehicle	High	Jul 7, 2026 Recall: Jul 7, 2026	Details
Improper Illumination of Towing Lights/FMVSS 108 Harbor Freight Tools (HFT) is recalling certain Kenway 12V LED Towing Light Kits with part number 64282, manufactured November 13, 2019 to December 22, 2019, and 12V Submersible Lights with part number 64274, manufactured July 1, 2019 to July 8, 2019. The lights may not illuminate properly. As such, these lights fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Assoc. Equipment." Improper illumination from the towing lights can reduce trailer visibility to other drivers, increasing the risk of a crash.	NHTSA 26E043000	Vehicle	High	Jul 7, 2026 Recall: Jul 7, 2026	Details
Incorrect Load Carrying Capacity Modification Label/FMVSS 110 Southeast Toyota Distributors, LLC (SET) is recalling one 2026 Tundra truck. The current load carrying capacity modification label is incorrect. As such, this vehicle fails to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." An incorrect load carrying capacity modification label may lead to improper loading of the vehicle, increasing the risk of a crash.	NHTSA 26V433000	Vehicle	High	Jul 6, 2026 Recall: Jul 6, 2026	Details
Vevor Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for Infant Sleep Products This recall involves VEVOR baby loungers. The recalled baby loungers are made of a foam sleeping pad and padded bumpers with a cloth cover and have a ribbon at one end. They were sold in the following colors and prints: snow deer, good night, forest friends (oval), forest friends (backpack), and green.?"VEVOR" is printed on an attached tag on the outside of the baby lounger's cover.	CPSC 10841	Child/Baby	High	Jul 3, 2026 Recall: Jul 2, 2026	Details
Topyond Pool Drain Ports with Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold by Jialyduu This recall involves Topyond white pool drain port with cover, sold as a Port Replacement Drainer for swimming pools. The plastic unit comes in a cardboard box with "SP-2850V" printed in bold, and a label which reads: "X004F4YG5X, Topyond Pool Drain Port Repl. MADE IN CHINA". Included in the box are stainless steel screws. The Topyond Pool Drain Port measures 9.1 inches by 6.7 inches and has a 2.3-inch opening for connection. There is no labeling or product identification on the product itself.	CPSC 10842	Consumer Product	High	Jul 3, 2026 Recall: Jul 2, 2026	Details
Projecting LED Finger Light Toys Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by POPOOO This recall involves POPOOO Jungle Safari LED Finger Lights. They were sold in sets of 24 multi-colored lights with white fingertip covers. Each finger light has three internal button cell batteries that power projections of the jungle safari characters when activated. "POPOOO" and "LED FINGER LIGHTS" are printed on the product's blue packaging.	CPSC 10844	Child/Baby	High	Jul 3, 2026 Recall: Jul 2, 2026	Details
Junpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Federal Statute for Child-Resistant Packaging of Coin Batteries; Sold on Amazon by JSNJ_Tech Store This recall involves Junpower CR2032 Batteries (20 pieces) in specific packaging (Packaging model 2023-V3). The product is packaged in a white box labeled "JUNPOWER Household Batteries," with four packs inside, each pack contains five batteries.	CPSC 10849	Child/Baby	High	Jul 3, 2026 Recall: Jul 2, 2026	Details
Diamond Wipes International Recalls CVS Health Medicated Hemorrhoidal Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging This recall involves CVS Health Medicated Hemorrhoidal Wipes. The pain-relieving wipes were sold in boxes of 20 individually wrapped packets of flushable wipes. The CVS Health logo, a yellow heart, "Rapid Pain Relief" and "Medicated Hemorrhoidal Wipes" is printed on the front of the packet and the box.	CPSC 10843	Child/Baby	High	Jul 3, 2026 Recall: Jul 2, 2026	Details
AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions; Sold on Amazon by Pretty-Life This recall involves AMASKY Nursing Pillows. The nursing pillows are C-shaped and sold in white with a crocodile pattern as well as other various colors and patterns. "Brand: AMASKY," "Model No.: BXP99/BXP93/BXP94/BXP96/BXP97" and "Batch Number: 202506001" are printed on a label attached to the pillow.	CPSC 10846	Child/Baby	High	Jul 3, 2026 Recall: Jul 2, 2026	Details
Rear Seat Belts May Not Secure Child Seat/FMVSS 208 Nissan North America, Inc. (Nissan) is recalling certain 2026 LEAF vehicles. The outer rear seat belt automatic locking retractors (ALR) may deactivate early, which can prevent a child restraint system (CRS) from securing properly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 208, "Occupant Crash Protection." An improperly secured child restraint system may not restrain an occupant as intended, increasing the risk of injury during a crash.	NHTSA 26V425000	Vehicle	High	Jul 2, 2026 Recall: Jul 2, 2026	Details
Park Outside: High Voltage Battery May Catch Fire Kia America, Inc. (Kia) is recalling certain 2022-2024 EV6 and 2024 EV9 vehicles. The high voltage battery cells may contain misaligned electrodes, which can lead to a fire while parked or driving. A fire increases the risk of injury.	NHTSA 26V431000	Vehicle	High	Jul 2, 2026 Recall: Jul 2, 2026	Details

Showing 151 - 175 of 3,083 product recalls

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Browse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.

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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Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.

UPC, Lot Code And Dates

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Model, Serial Or Date Code

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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

Consumer Product Recalls

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FDA

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FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.

USDA FSIS

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Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.

NHTSA

Vehicle, Tire And Car Seat Recalls

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.

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

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