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.
Start with the product name or brand. If the list is too broad, search the exact UPC, lot code, model number, date code, NHTSA campaign number or official recall number printed on the notice or label.
Results help you find a possible match quickly. Before you stop use, discard, return or repair anything, open the official notice and confirm every affected detail.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1444-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization system, Product Number TSMICS1
During the manufacturing, 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-1473-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Jan 13, 2026
|
Details |
|
Olympus Resection Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. Resection sheath for urologic applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1439-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1447-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Olympus Resection Sheath, 28 Fr. with Deflecting Obturator. Model No. A22043T. Resection sheath for urologic applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1446-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Olympus Inner Sheath. Model No. A2641. for endoscopic diagnosis and treatment in urological applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1455-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1445-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Convenience kits used for dialysis maintenance Medline ADD A CATH DIALYSIS KIT SKU ECVC8415A Centurion CENTRAL LINE INSERTION TRAY SKU DT19810 Centurion DIALYSIS BUNDLE WITH NO CATHETTER SKU CVI4310A Medline DIALYSIS CAP CHANGE KIT SKU DYNDC2425 Medline DIALYSIS CHANGE KIT SKU EBSI1453A Centurion HEMODIALYSIS ACCESS KIT SKU DT12970 Medline LARGE BORE, DIALYSIS, ENHANCED SECUREMENT SKU EBSI1741
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
|
FDA
Z-1465-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Jan 8, 2026
|
Details |
|
Olympus Inner Sheath, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1450-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with SL-110, Mobile Exam Light
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
|
FDA
Z-1436-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Oct 13, 2025
|
Details |
|
Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1442-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Model/Catalog Number: 509-00-432
Knee and Humeral socket implants contain incorrect labeling.
|
FDA
Z-1458-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Jan 15, 2026
|
Details |
|
Olympus Sheath, 10 Fr. Model No. A37004A. for endoscopic diagnosis and treatment in urological applications.
Complaints of the ceramic tip of the resection sheath breaking have been received.
|
FDA
Z-1454-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Nov 11, 2025
|
Details |
|
Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU DYNDC3167
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
|
FDA
Z-1468-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Jan 8, 2026
|
Details |
|
Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
|
FDA
Z-1464-2026
|
Medical Device | High |
Mar 4, 2026
Recall: Jan 8, 2026
|
Details |
|
FDA
H-0519-2026
|
Food | High |
Mar 4, 2026
Recall: Feb 3, 2026
|
Details | |
|
Mung Beans packaged in 4lb polybags; 6-4lb bags per carton
Presence of Thiamethoxam-PESTICIDE
|
FDA
H-0524-2026
|
Food | High |
Mar 4, 2026
Recall: Jan 15, 2026
|
Details |
|
FDA
H-0534-2026
|
Food | High |
Mar 4, 2026
Recall: Feb 6, 2026
|
Details | |
|
FDA
H-0522-2026
|
Food | High |
Mar 4, 2026
Recall: Feb 12, 2026
|
Details | |
|
Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
|
FDA
H-0527-2026
|
Food | High |
Mar 4, 2026
Recall: Nov 21, 2025
|
Details |
|
Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged in a plastic resealable bag with UPC 015000005962, packed 4 bags/case with UPC 015000935726; Made for Gerber Products Co., Fremont, MI 49413
Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
|
FDA
H-0518-2026
|
Food | High |
Mar 4, 2026
Recall: Jan 26, 2026
|
Details |
|
Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
|
FDA
H-0528-2026
|
Food | High |
Mar 4, 2026
Recall: Nov 21, 2025
|
Details |
|
Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label is read in parts: ***INGREDIENTS: Sugar***Whey Powder, Nonfat Milk Powder, Soy Lecithin***Peanut Butter (peanuts, peanut oil***), Pretzels (wheat flour***buttermilk solids***CONTAINS MILK AND SOY ***May contain wheat, peanuts and tree nuts***"
Ingredients List declares peanut but the Contains statement does not declare peanut
|
FDA
H-0523-2026
|
Food | High |
Mar 4, 2026
Recall: Jan 30, 2026
|
Details |
|
Valley Springs Steamed Distilled Water. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-00601 2. Bottled by Valley Springs/Artesian Gold, LLC, Portage WI 53901.
Water was bottled under insanitary conditions.
|
FDA
H-0536-2026
|
Food | High |
Mar 4, 2026
Recall: Feb 6, 2026
|
Details |
|
Yoyo Gummy Grape Plus Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
|
FDA
H-0529-2026
|
Food | High |
Mar 4, 2026
Recall: Nov 21, 2025
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
Cars & equipmentSearch 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 updatesBrowse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.
Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.
For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.
This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.
Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.
FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.
Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.
Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.
Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.
Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.
Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.
The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.
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.
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.
Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.
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.
A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.
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.
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.
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.
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.
Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.
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.
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.