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

Latest Product Recall Matches

Showing 276 - 300 of 3,083 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435. Potential for thrombus formation during prolonged use of the introducer.	FDA Z-2600-2026	Medical Device	High	Jul 1, 2026 Recall: May 22, 2026	Details
Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476 Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.	FDA Z-2531-2026	Medical Device	High	Jul 1, 2026 Recall: May 20, 2026	Details
Octopus Evolution AS Tissue Stabilizer, Model TS2500 During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.	FDA Z-2576-2026	Medical Device	High	Jul 1, 2026 Recall: May 12, 2026	Details
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2572-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2561-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.	FDA Z-2522-2026	Medical Device	High	Jul 1, 2026 Recall: May 26, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CRANIOTOMY PACK-LF DYNJ0101292F DYNJ0101292G HYBRID PACK DYNJ65925A LAMINECTOMY DYNJ905156L DYNJ905156M DYNJ905156N DYNJ905156O DYNJ905156P MAJOR EXTREMITY DYNJ905159F DYNJ905159I DYNJ905159J DYNJ905159K NEURO CERVICAL PACK DYNJ0101287J DYNJ0101287K NEURO SPINE PACK DYNJ81612C POSTERIOR SPINE PACK-LF DYNJ0843339L DYNJ0843339M DYNJ0843339N SPINE PACK DYNJ30150F Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.	FDA Z-2587-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2562-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834. Potential for thrombus formation during prolonged use of the introducer.	FDA Z-2601-2026	Medical Device	High	Jul 1, 2026 Recall: May 22, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO PACK DYNJ30565C DYNJ32555B ANGIO PACK-LF DYNJ0774765U ANGIO TRAY DYNJ46153A ANGIOGRAM TRAY DYNJ33638K ANGIOGRAPHY DRAPE PK QVH-LF DYNJ35110D ANGIOGRAPHY PACK DYNJ44293D ANGIOGRAPHY PACK-LF DYNJ0854485T DYNJ35916J GENERAL ANGIO PACK DYNJ57760B GENERAL ENDO PACK-LF DYNJ0842873J JUDKINS PACK DYNJ51126A RADIOLOGY ANGIO MAJOR PACK DYNJ62858B TAVR JUDKINS PACK DYNJ51127B Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.	FDA Z-2591-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR VASCULAR PACK DYNJ81610C MINIMALLY INVASIVE PACK-LF DYNJ0843063L PEDIATRIC CATH ANGIO PACK DYNJ54755J PERIPHERAL ARTERIOGRAM RAD DYNJ61383C POSTERIOR SPINE PACK-LF DYNJ0843339O UPPER EXTREMITY DYNJ61907A VISCERAL ANGIOGRAM PACK-LF DYNJ0429121L Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.	FDA Z-2590-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details
VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001 Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.	FDA Z-2525-2026	Medical Device	High	Jul 1, 2026 Recall: May 8, 2026	Details
Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241 Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.	FDA Z-2528-2026	Medical Device	High	Jul 1, 2026 Recall: May 20, 2026	Details
Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2558-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US Retail Sensor/Transmitter 1-pack Model/Catalog Number: STP-AT-012 Software Version: N/A Product Description: Dexcom G7 US Retail Sensor/Transmitter 1-pack Component: Dexcom G7 Continuous Glucose Monitoring System Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were later sold to pharmacies and distributors by Pharmsource, LLC. Lot 1725204004 were designated for destruction because the G7 sensors were not properly sterilized and have an increased risk of skin infection if used. Lot 1725069002 were designated for destruction due to an increased risk of having no sensor readings available or experiencing sensor inaccuracy that includes the potential for missed detection of a hyperglycemic event or incorrect treatment decisions that can result in patient injury, including medical intervention to prevent permanent injury or impairment. Additionally, due to the unknown storage and handling and storage conditions these sensors may have undergone during the distribution, these sensors may present additional risk.	FDA Z-2574-2026	Medical Device	High	Jul 1, 2026 Recall: May 27, 2026	Details
Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2568-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Gear Position Indicator Not Displayed/FMVSS 102 Chrysler (FCA US, LLC) is recalling certain 2022-2024 Jeep Grand Cherokee, 2023 Jeep Wagoneer, 2024 Jeep Grand Cherokee L, and Jeep Wagoneer L vehicles. A software error may cause the transmission gear selection indicator not to display. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission shift lever sequence, starter interlock, and transmission braking effect." A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.	NHTSA 26V413000	Vehicle	High	Jun 30, 2026 Recall: Jun 30, 2026	Details
Loss of Electronic Stability Control & Brake Assist/FMVSS 126 & 135 Chrysler (FCA US, LLC) is recalling certain 2026 Jeep Grand Wagoneer and Jeep Grand Wagoneer L vehicles. The brake system control module software may cause a loss of electronic stability control and a loss of electronic brake assist. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 126, "Electronic Stability Control Systems" and 135, "Light Vehicle Brake Systems." A loss of electronic stability control and/or electronic brake assist increases the risk of a crash.	NHTSA 26V414000	Vehicle	High	Jun 30, 2026 Recall: Jun 30, 2026	Details
Instrument Panel May Fail to Display Selected Gear/FMVSS 102 Nissan North America, Inc. (Nissan) is recalling certain 2026 Rogue vehicles. The instrument panel may not display the transmission gear selection indicator. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission Shift Lever Sequence, Starter Interlock, and Transmission Braking Effect." A missing gear selection indicator may lead to unintended vehicle movement or a vehicle rollaway, increasing the risk of a crash.	NHTSA 26V419000	Vehicle	High	Jun 30, 2026 Recall: Jun 30, 2026	Details
Rear Differential Pinion Shaft May Fracture Ford Motor Company (Ford) is recalling certain 2021-2023 Mustang Mach E vehicles. The rear differential pinion shaft may fracture. Differential pinion shaft fracture may result in a loss of drive power, or unintended vehicle movement if the vehicle is in park without the parking brake applied, increasing the risk of a crash.	NHTSA 26V417000	Vehicle	High	Jun 30, 2026 Recall: Jun 30, 2026	Details
Windshield Wiper and Washing System Malfunction Ford Motor Company (Ford) is recalling certain 2024-2026 Mustang and 2025-2026 Mustang GTD vehicles. During certain cold temperature conditions, the windshield wipers may function only at their high-speed setting and the washing system may fail to function properly. Windshield wipers or a washing system that fails to function as intended can reduce visibility, increasing the risk of a crash.	NHTSA 26V418000	Vehicle	High	Jun 30, 2026 Recall: Jun 30, 2026	Details
Instrument Panel May Fail to Display Selected Gear/FMVSS 102 Nissan North America, Inc. (Nissan) is recalling certain JATCO transaxle assembly automatic transmission part numbers 31020X274D, 31020X275A, 3102MX274CRE, 3102MX275ARE, 3102MX275BRE, and 3102MX275DRE. An internal hardware failure within the control valve assembly's inhibitor switch may cause the instrument panel to improperly display the transmission gear shifter indicator. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission Shift Lever Sequence, Starter Interlock, and Transmission Braking Effect." An instrument panel display that does not show critical information, such as gear selection, increases the risk of a crash.	NHTSA 26E039000	Vehicle	High	Jun 30, 2026 Recall: Jun 30, 2026	Details
Missing Pedestrian Warning Sounds/FMVSS 141 Teko Inc (Teko) is recalling certain 2026 Triumph, Turbo, TurboLite, Trophy, and Trophy Plus vehicles. The acoustic vehicle alerting system (AVAS) may not have been installed, preventing the vehicle from making pedestrian warning sounds. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 141, "Minimum Sound Requirements for Hybrid and Electric Vehicles." A vehicle that does not make a sound may fail to alert pedestrians of an approaching vehicle, increasing the risk of a crash or injury.	NHTSA 26V420000	Vehicle	High	Jun 30, 2026 Recall: Jun 30, 2026	Details
Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash; Violate Mandatory Standard for ATVs This recall involves XW-A17 Electric Youth ATVs sold under brand names including Sunderwell in blue, green, orange and pink. "Model:XW-A17" is printed on the identification plate located on the front left side of the frame column. "Yamazuki, Inc. certifies that this ATV complies with ANSI/SVIA 1-2023 Standard. "This ATV is subject to the Yamazuki, Inc. ATV Action Plan filed with and approved by the U.S. Consumer Product Safety Commission" is also printed on the identification plate.	CPSC 10832	Consumer Product	High	Jun 30, 2026 Recall: Jun 25, 2026	Details
Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Additional Model and Reported Incidents This recall involves the Lomi Roll-On Waxing Kit with Wax Cartridge & Wax Strips, model numbers LOMB2003PK and LOMB2004PK. The recalled boxed kits included a handheld wax warmer, a wax cartridge, wax strips, a power cord and a user's manual. The Lomi logo is printed on the front of the white and pink warmer and on the outside of the product packaging. The model number is printed on a label on the bottom of the wax warmer.	CPSC 10834	Consumer Product	High	Jun 30, 2026 Recall: Jun 25, 2026	Details

Showing 276 - 300 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.

Product Name Or Brand

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

For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.

Model, Serial Or Date Code

For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.

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

The goal is to make official notices easier to search. The final decision should still come from the linked agency or manufacturer notice.

CPSC

Consumer Product Recalls

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FDA

Food And Medical Device Recalls

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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