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 |
|---|---|---|---|---|---|
|
Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
|
FDA
Z-2559-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Apr 30, 2026
|
Details |
|
Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a patient's vasculature could result in localized inflammation and tissue irritation.
|
FDA
Z-2526-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Apr 21, 2026
|
Details |
|
Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM SET UP
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
|
FDA
Z-2452-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 6, 2026
|
Details |
|
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO DRAPE PACK (ADLUG)642-LF DYNJ47665D ANGIO PACK DYNJ30565D ANGIOGRAPHY PACK-LF DYNJ0854485V ARTERIOGRAM DYNJ28082D DYNJ28082F CARDIAC CATH DYNJ67349 CARDIAC CATH PACK DYNJ57874C CATH I PLUS-LF DYNJSCL100 CATH III PLUS-LF DYNJSCL300 CATH LAB ANGIOGRAPHY PACK DYNJ50779F CATH LAB PACK DYNJ41088B DYNJ48085 CATH LAB TRAY DYNJ37389N DYNJ37389O CATH PACK DYNJ62595A DYNJ69997 EP DRAPE PACK-LF DYNJ47645B HOSPITAL REGIONAL DE CONCEPCIO DYNJ67918A INTERVENTIONAL PACK DYNJ56666C INTERVENTIONAL RAD PACK DYNJ44100L INTERVEN
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-2592-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Feb 27, 2026
|
Details |
|
Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
|
FDA
Z-2557-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Apr 30, 2026
|
Details |
|
Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000434. Introducer Product Code: 1000434.
Potential for thrombus formation during prolonged use of the introducer.
|
FDA
Z-2599-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 22, 2026
|
Details |
|
Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Size 9, 9+ 10mm Thicknes Component: N/A
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
|
FDA
Z-2578-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 11, 2026
|
Details |
|
Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Software anomaly that causes a false display of error code 5018.
|
FDA
Z-2554-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 5, 2026
|
Details |
|
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
|
FDA
Z-2580-2026
|
Medical Device | High |
Jul 1, 2026
Recall: May 11, 2026
|
Details |
|
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO CATH COMBINED PACK DYNJ43609S ANGIO PACK DYNJ67987D DYNJ80317A ANGIO SPECIAL PROCEDURE-LF DYNJ38412C ANGIOGRAM SET UP PACK DYNJ66260A ANGIOGRAPHY PACK DYNJ44293I ANGIOGRAPHY PACK-LF DYNJ0854485W CARDIAC CATH PACK DYNJ82709 CARDIAC CATH PACK-LF DYNJ0261554AL DYNJ31103F CATH LAB ANGIO TRAY DYNJ83506 CATH LAB PACK DYNJ66366C MSC-GREEN BAY ST VINCENT SAMPC0686 NEUROLOGICAL CATH PACK DYNJ63434B OR HYBRID-MRMC DYNJ907758B STEWARD OR ANGIO PACK GSS DYNJ80925B
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-2582-2026
|
Medical Device | High |
Jul 1, 2026
Recall: Feb 27, 2026
|
Details |
|
8/9.5oz Tub Nut - Sunflower Seed
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
|
FDA
H-1120-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 29, 2026
|
Details |
|
5# Sunflower Seeds C/S
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
|
FDA
H-1121-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 29, 2026
|
Details |
|
Joy Orange Lassi 16 oz.
Product not adequately pasteurized
|
FDA
H-1093-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 23, 2026
|
Details |
|
FDA
H-1106-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
FDA
H-1124-2026
|
Food | High |
Jul 1, 2026
Recall: May 13, 2026
|
Details | |
|
FDA
H-1096-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
1.5oz, 8.0oz , Zapp's Big Cheezy Potato Chips, Plastic Bag.
Potential presence of Salmonella.
|
FDA
H-1116-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 28, 2026
|
Details |
|
FDA
H-1105-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
FDA
H-1098-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and covered entirely in transparent, flexible plastic wrap. (20 bonbon pieces per 400g box). UPC 5304000050757
Undeclared colors (FD&C Yellow 5 and FD&C Red 40).
|
FDA
H-1110-2026
|
Food | High |
Jul 1, 2026
Recall: May 21, 2026
|
Details |
|
Joy Strawberry Lassi 16 oz.
Product not adequately pasteurized
|
FDA
H-1086-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 23, 2026
|
Details |
|
FDA
H-1097-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
Joy Mango Lassi 16 oz., 64 oz.
Product not adequately pasteurized
|
FDA
H-1081-2026
|
Food | High |
Jul 1, 2026
Recall: Apr 23, 2026
|
Details |
|
FDA
H-1099-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
Details | |
|
FDA
H-1104-2026
|
Food | High |
Jul 1, 2026
Recall: Jan 9, 2026
|
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.