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

Latest Product Recall Matches

Showing 3,151 - 3,175 of 3,318 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Allura Xper FD10/10; Model Number: 722011; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1069-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System. AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.	FDA Z-1040-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 4, 2025	Details
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) PRE OP KIT, Medline kit SKU DYKS1093B; 2) PRE OP KIT, Medline kit SKU DYKS1124C; 3) PRE OP KIT, Medline kit SKU DYKS1128C; 4) PREOP KIT, Medline kit SKU DYKS1130B; 5) PRE OP KIT, Medline kit SKU DYKS1163G; 6) PRE OP KIT SURGERY, Medline kit SKU DYKS1263G; 7) PREOP KIT, Medline kit SKU DYKS1313A; 8) PRE OP KIT, Medline kit SKU DYKS1325A; 9) ADULT PRE OP KIT, Medline kit SKU DYKS1337D; 10) PRE OP KIT ADULT, Medline kit SKU DYKS1362A; 11) PRE-OP - OUTPATIENT KIT, Medline kit SKU DYKS1378B; 12) PRE Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.	FDA Z-1057-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 26, 2025	Details
Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE, REF CDS980754T; 2) GYN LAP HYSTERECTOMY CDS, REF CDS982662Q; 3) DAVINCI HYSTERECTOMY CDS, REF CDS985344F; 4) LAVH, REF DYNJQ9041R; 5) LAPAROSCOPIC HYSTERECTOMY, REF DYNJ900244I; 6) ROBOTIC LAVH, REF DYNJ901281I; 7) LAVH-LF, REF DYNJ901829T; 8) LEX LAP HYST, REF DYNJ902030J; 9) LITHOTOMY-SLINGS-LF, REF DYNJ905274D; 10) GYN LAPAROSCOPY, REF DYNJ905485J; 11) ROBOTIC HYSTERECTOMY, REF DYNJ906380C; 12) LAPAROSCOPIC HYSTERECTOMY, REF DYNJ910634; 13) LAVH GYN/ONC, REF DYNJ910927. Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.	FDA Z-1089-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 16, 2025	Details
Allura Xper FD10; Model Number: 722003; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1064-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5. Azurion 7 B12. Model Number: 722235. 6. Azurion 7 B20. Model Number: 722236. 7. Azurion 7 M12. Model Number: 722233. 8. Azurion 7 M20. Model Number: 722234. Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on the FlexVision monitor, system continues to restart, AMD triple drive, C-Partition of Suite PC running out of free space, system remains in continuous restart mode after start-up, misalignment of Marker Tool Overlay, longitudinal position error.	FDA Z-1079-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 8, 2025	Details
Product Name: Allura Xper FD10C; Model number: 722001; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1062-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Allura Xper FD20; Model Number: 722028; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1075-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Allura Xper FD10/10; Model Number: 722027; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1074-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B; 2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B; 3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C; 4) TOP DRAWER #6, Medline kit SKU ACC010688; 5) RRMC CODE CART DRAWER 3, Medline kit SKU ACC010770; 6) SURGERY BAG, Medline kit SKU DYKM1279C; 7) ADMISSION KIT, Medline kit SKU DYKS1179; 8) PRE OP KIT, Medline kit SKU DYKS1192C; 9) MEDLINE PEDIATRIC PATIENT PACK, Medline kit SKU DYKS1199B; 10) MEDLINE ADULT PATIENT PACKAGE, Medli Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.	FDA Z-1055-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 26, 2025	Details
Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174 Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant.	FDA Z-1039-2026	Medical Device	High	Jan 21, 2026 Recall: Oct 29, 2025	Details
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900). Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.	FDA Z-1043-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 3, 2025	Details
Brand Name: PALACOS Product Name: PALACOS R+G pro 40; PALACOS R+G pro 80 Model/Catalog Number: 5081288; 5081289 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.	FDA Z-1081-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 9, 2025	Details
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL PACK, Medline kit SKU DYNJ54488A Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.	FDA Z-1054-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 26, 2025	Details
Allura Xper FD10F; Model Number: 722002; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1063-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F Labeling error, Incorrect expiration date	FDA Z-1061-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 29, 2025	Details
da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box) Access Port System tray may develop cracks potentially resulting in a sterility breach.	FDA Z-1096-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.	FDA Z-1090-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 16, 2025	Details
VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 There is a potential for formation of ice occurring in the venting system of the superconducting magnet of the MRI systems. if a quench occurs in this condition, helium gas may not be able to escape via the designed vent paths, and the pressure in the helium vessel may rise. This pressure build-up could eventually rupture the helium vessel, causing helium gas to be released into the MR scanning room.	FDA Z-1017-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 19, 2025	Details
MOSAIQ Oncology Information System with Particle Therapy License (License Kit 45700000000IQRO) Using oncology information system that manages workflow may result in overtreatment if:Plan delivered with Particle Therapy IHE-RO TDW-II interface,With one field per fraction or last field partial treatment,Partial treatment occurs followed by treatment field interruptions with manually recorded partial treatment,Then treatment unit doesn't check meterset value so partial treatment delivered twice	FDA Z-1078-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 10, 2025	Details
HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4 Potential undeclared allergen ingredient (Wheat)	FDA H-0405-2026	Food	High	Jan 21, 2026 Recall: Jan 6, 2026	Details
2248 Banana Pudding Ice Cream, 3 GAL, UPC 7 65265 81237 8 Undeclared soy lecithin	FDA H-0383-2026	Food	High	Jan 21, 2026 Recall: Dec 12, 2025	Details
Cinnamon, Clear Plastic Container, 100G, UPC 6251136 034139 Elevated levels of lead.	FDA H-0388-2026	Food	High	Jan 21, 2026 Recall: Sep 9, 2025	Details
So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert, One Pint (473 mL). UPC 744473 476138. Manufactured By/For So Delicious Dairy Free Eugene, OR 97402 So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. Net wt. 500mL. UPC 744473 276134. Product of the U.S.A. Distributed by Danone Inc., Boucherville, Quebec J4B 1E6 Foreign material	FDA H-0398-2026	Food	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Publix Rice & Pigeon Peas, Net Wt 32 oz (2lb), Plastic tray with clear lid, black film, and a pre-printed label. 6 (2lb) containers per case . Undeclared Allergen (Soy)	FDA H-0385-2026	Food	High	Jan 21, 2026 Recall: Dec 16, 2025	Details

Showing 3,151 - 3,175 of 3,318 product recalls

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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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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

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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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