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

Q: 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.

Q: 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.

Q: 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.

Q: 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.

Latest Product Recall Matches

Showing 3,076 - 3,100 of 4,622 matching product recalls.

Open Latest Recalls

Product Recall	Source	Type	Risk	Date	Action
MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous Access Device permits short-term (<30 days) venous access and catheter introduction to the central circulation. Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured	FDA Z-1916-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 11, 2026	Details
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes JUDKINS PACK DYNJ51126 ANGIO PACK DYNJ32555C, DYNJ66631 ANGIO TRAY DYNJ46153B ANGIOGRAPHY PACK DYNJ26855F ANGIOGRAPHY PACK-M-LF DYNJ24530I ANGIOGRAPHY TRAY-LF DYNJ0220880V, DYNJ30077D CATH LAB ANGIO PACK-LF DYNJ0545064X CATH LAB PACK DYNJ39057C FEMORAL ANGIOGRAPY SET UP DYNJ61015B RAD-ANGIO PACK DYNJ47710C SURGERY ANGIO PACK-LF PHS677784013A Unapproved design changes to the products outside of the 510(k) clearance.	FDA Z-1876-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 27, 2026	Details
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC. Potential for detachment of a distal tip component of the device during use.	FDA Z-1851-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 23, 2026	Details
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UPN No.: H787107140215 (Box), H787107140210 (Pouch); Box Quantity: 5 pouches; The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.	FDA Z-1866-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 3, 2026	Details
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BASIC CL PACK-LF DYNJ87052 BASIC PACK DYNJ83976 BASIC SET UP PACK DYNJ80700 CORONARY ANGIOGRAPHY PACK (N) DYNJ42136B CSTM ANGIO KIT - S VASC1109 CV PACK DYNJ46301C DR F PACK DYNJ41253B ENSEMBLE HEMORROIDES DYNJ56311A G TAVR PACK DYNJ61006 IR MINOR PACK DYNJ44139C MAJOR PLUS PACK DYNJ905160N MAXIMUM BARRIER BUNDLE PACK DYNJ35216C PCI PACK TBRHSC-LF DYNJ41941D PERC PACK-LF DYNJ0774759P PERIPHERAL ANGIOGRAPHY PK DYNJ42094B PR Unapproved design changes to the products outside of the 510(k) clearance.	FDA Z-1883-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 27, 2026	Details
LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555 Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.	FDA Z-1930-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 9, 2026	Details
Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog No.: 10714016; Product/UPN No.: H787107140165 (Box), H787107140160 (Pouch); Box Quantity: 5 pouches; The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.	FDA Z-1863-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 3, 2026	Details
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B ANGIO PHC DYNJ37485C C.I.C.N. ANGIO PACK DYNJ53064B FHT P NEURO PACK DYNJ39931D NEURO ARTERIOGRAM PACK-LF DYNJ0948060F NEURO KIT NAM0003 NEURO PACK DYNJ61542D NEURO RADIOLOGY PACK DYNJ59903B NEURO TRAY DYNJ84872A PK, CATH LAB-ANGIO DYNJ44027F QVH IR NEURO PACK DYNJ62176 Unapproved design changes to the products outside of the 510(k) clearance.	FDA Z-1884-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 27, 2026	Details
Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK, Model Number: DYNJT2021G; 3) ANGIOGRAPHY PACK, Model Number: DYNJ31377B; 4) ANGIO PACK, Model Number: DYNJ51279; 5) ANGIOGRAPHY PACK II, Model Number: DYNJ52447; 6) CATH ANGIO PACK, Model Number: DYNJ53369C; 7) ANGIO PACK, Model Number: DYNJ53591A; 8) ANGIOGRAPHIC PACK, Model Number: DYNJ57516; 9) ANGIOGRAPHY TRAY-LF, Model Number: DYNJ58722A; 10) ANGIO TRAY W/CHLORAPREP, Model Number: DYNJ62742; 11) CEREBRAL ANGIOGRAM, Model Number: DYNJ67876; 12) CSU CATH MANIFOLD KIT, Model Number: VASC1170A The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.	FDA Z-1834-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 25, 2026	Details
Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Number: DYNDH2104; 3) CARDIAC CATH PACK-LF, Model Number: DYNJT2164M; 4) ANGIOGRAPHY TRAY, Model Number: DYNJT3078; 5) CATH PACK, Model Number: DYNJT4190; 6) ANGIO VASCULAR PACK, Model Number: DYNJT5717; 7) HEART CATH PACK, Model Number: DYNJ0381139R; 8) CARDIAC CATH PACK, Model Number: DYNJ04529L; 9) CUSTOM RADIOLOGY PACK, Model Number: DYNJ07955L; 10) STVZ CARDIAC CATH PACK, Model Number: DYNJ24619J; 11) CATH TRAY #2, Model Number: DYNJ24706D; 12) CATH LAB PACK, Model Number: DYNJ24802Q; 13) CATH PACK, Model Number: D The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.	FDA Z-1835-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 25, 2026	Details
LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554 Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.	FDA Z-1933-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 9, 2026	Details
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115. XXX	FDA Z-1903-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 25, 2026	Details
AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM; Catalog No.: 13709604; Product/UPN No.: H787137096045 (Box), H787137096040 (Pouch); Box Quantity: 5 pouches; The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.	FDA Z-1873-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 3, 2026	Details
Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG S, Model Number: DYNJHWIRE105; 3) GWIRE HYDRO 0.035 260CM ANG S, Model Number: DYNJHWIRE107; 4) GWIRE HYDRO 0.035 260CM STR S, Model Number: DYNJHWIRE115; 5) GWIRE HYDRO 0.035 150CM STR, Model Number: DYNJHWIRE108; 6) GWIRE HYDRO 0.035 150CM ANG S, Model Number: DYNJHWIRE104; 7) GWIRE HYDRO 0.035 180CM STR S, Model Number: DYNJHWIRE113; 8) GWIRE HYDRO 0.035 260CM ANGLE, Model Number: DYNJHWIRE103; 9) GDWIRE .035INX150CM 3MMJ LT, Model Number: DYNJGWIRE01L; 10) GDWIRE .035INX18 The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.	FDA Z-1829-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 25, 2026	Details
Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC. Potential for detachment of a distal tip component of the device during use.	FDA Z-1854-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 23, 2026	Details
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes TAVR PACK DYNJ69246B ABDOMINAL VASCULAR-LF DYNJ905291D ANGIOGRAPHIC PACK DYNJ86769 AORTAGRAM PACK DYNJ26783D AV FISTULA PACK CHS-LF DYNJ35615G AV SHUNT PACK-LF DYNJ0842516G CATHETER PACK DYNJ61926 EP DRAPE PACK-LF DYNJ47645C EP PACK DYNJ47782G EPS ACCESSORY PACK DYNJT2201S H CLINIC VASCULAR PK DYNJ33415A HEART FAILURE PACK DYNJ64877B HYBRID PACK DYNJ65925D INTERVENTIONAL RAD PACK DYNJ44100M INTERVENTIONAL RADIOLOGY PK-LF DYNJ0516014AG MV-PACEMAKER PACK-LF DYNJ41556F NEURO RADIOLOGY RICHMOND DYNJ68365D OR HYB Unapproved design changes to the products outside of the 510(k) clearance.	FDA Z-1878-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 27, 2026	Details
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ909398A ROBOTIC PACK DYNJ908706D Unapproved design changes to the products outside of the 510(k) clearance.	FDA Z-1885-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 27, 2026	Details
Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model Number: DYNJ37543A The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.	FDA Z-1838-2026	Medical Device	High	Apr 29, 2026 Recall: Feb 25, 2026	Details
Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (Box), H787107140140 (Pouch); Box Quantity: 5 pouches; The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.	FDA Z-1862-2026	Medical Device	High	Apr 29, 2026 Recall: Mar 3, 2026	Details
Pop-Top Latch and Safety Straps May Fail Roadtrek Inc. (Roadtrek) is recalling certain 2024-2026 Westfalia Wave SL, 2022-2026 Zion Slumber, Play Slumber, 2026 Play Tuff SL, 2025-2026 Play+Slumber, and 2024 Pivot Slumber recreational vehicles. The pop-top latch may disengage during transit, causing the pop-top to lift. A pop-top that lifts during transit can distract the driver, or detach if the secondary safety straps fail, increasing the risk of a crash.	NHTSA 26V271000	Vehicle	High	Apr 29, 2026 Recall: Apr 29, 2026	Details
Front Chin Spoiler May Detach During Transit Newmar Corporation (Newmar) is recalling certain 2026 Freedom Aire motorhomes. The front chin spoiler may detach during transit. A detached spoiler may become a road hazard, increasing the risk of a crash.	NHTSA 26V272000	Vehicle	High	Apr 29, 2026 Recall: Apr 29, 2026	Details
Incorrect Cargo Carrying Capacity on Label/FMVSS 120 Newmar Corporation (Newmar) is recalling certain 2026 Freedom Aire motorhomes. The Cargo Carrying Capacity (CCC) label may state an incorrect weight value. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, “Wheels and Rims - Other Than Passenger Cars.” Incorrect weight information can allow the vehicle to be overloaded, increasing the risk of a crash.	NHTSA 26V273000	Vehicle	High	Apr 29, 2026 Recall: Apr 29, 2026	Details
Detached Shift Cable Bushing/FMVSS 102, 114 Dorman Products, Inc. (Dorman) is recalling certain Dorman Transmission Gearshift Cables, with part numbers 905-146, 905-644, 905-142, and Solutions Transmission Gearshift Cables with part numbers BK905-1146-1, and BK905-1142-1. The gearshift cable bushing may detach from the linkage, which can prevent the vehicle from shifting into gear properly, including "Park" position. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) numbers 102, “Transmission shift position sequence, starter interlock, and transmission braking effect," and FMVSS number 114, "Theft Protection." The inability to shift into "Park" can result in a vehicle rollaway, increasing the risk of a crash.	NHTSA 26E024000	Vehicle	High	Apr 29, 2026 Recall: Apr 29, 2026	Details
Improperly Routed Coolant Lines May Cause a Loss of Drive Power Storyteller Overland, LLC (Storyteller) is recalling certain 2023 Stealth, Classic, and Beast Mode vehicles equipped with AWD. Improperly routed coolant lines may overheat the engine, causing a loss of drive power. A loss of drive power increases the risk of a crash.	NHTSA 26V274000	Vehicle	High	Apr 29, 2026 Recall: Apr 29, 2026	Details
Loose Bolt in Front Seat Frame Ford Motor Company (Ford) is recalling certain 2024-2026 Ranger and Bronco vehicles. The front seats may have a loose or dislodged seat frame height-adjust pivot bolt. A seat with a dislodged bolt may not properly restrain an occupant in a crash, increasing the risk of injury.	NHTSA 26V268000	Vehicle	High	Apr 28, 2026 Recall: Apr 28, 2026	Details

Showing 3,076 - 3,100 of 4,622 product recalls

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Food safety

Food Product Recall Search

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Vehicle Recall Lookup

Search campaigns by make, model, year, component or NHTSA number. Use NHTSA's VIN search for vehicle-specific open recall status.

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Fresh updates

Latest Product Recalls Today

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

Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.

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

Meat, Poultry And Egg Product Recalls

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?