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 |
|---|---|---|---|---|---|
|
Unprotected Boom Stow Wire May Short and Cause Fire
Altec Industries, Inc. (Altec) is recalling certain 2013-2025 AP45A trucks. The boom stow switch wire in the cargo storage area may become damaged, which can result in a short circuit, causing the wire to overheat. An overheated wire can ignite flammable material in the cargo area, increasing the risk of fire.
|
NHTSA
26V457000
|
Vehicle | Unknown |
Jul 16, 2026
Recall: Jul 16, 2026
|
Details |
|
Battery Cable May Short Circuit
International Motors, LLC (International) is recalling certain 2021, 2023-2027 MV, and 2026-2027 HV vehicles. The battery interconnect cable may contact the auxiliary stud and hold down bracket, causing a short circuit. A short circuit increases the risk of a fire.
|
NHTSA
26V459000
|
Vehicle | Unknown |
Jul 16, 2026
Recall: Jul 16, 2026
|
Details |
|
FDA
H-1142-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details | |
|
Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.
|
FDA
H-1148-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 25, 2026
|
Details |
|
High Valley Orchard Chocolate Covered Raisins, net wt. 15oz. per package, each case contains 12/15oz. bags. Product is packaged in clear plastic container. UPC on retail container: 0 952348 80170 0. The label of affected product declares: INGREDIENTS: MILK CHOCOLATE (SUGAR, ***WHOLE MILK POWDER, SOY LECITHIN ***RAISINS***CONTAINS MILK AND SOY*** Distributed by Lehi Valley Trading Company of Mesa, AZ.
Undeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.
|
FDA
H-1150-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details |
|
JB Chicken Sknls 35.73#
Undeclared Sesame allergen
|
FDA
H-1139-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual marshmallows packaged in a sealed plastic bag inside a printed cardboard box
Foreign material: small metal pieces
|
FDA
H-1147-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 11, 2026
|
Details |
|
Fresh to You Burger Chicken Fillet, SKU 10150, Net wt. 5oz. Product is refrigerated. UPC 1 00000 01015 0. Manufactured By LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Fillet sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.
|
FDA
H-1149-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 25, 2026
|
Details |
|
Coopers Bbq 60 Gal Bean Mix box
Undeclared Sesame allergen
|
FDA
H-1141-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
FDA
H-1145-2026
|
Food | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details | |
|
Trafa Pharmaceuticals Inc. brand ORGANIC MORINGA LEAF POWDER; NET WEIGHT: 15 KGS; packaged in brown paper bags with a white label
Potential contamination with Salmonella
|
FDA
H-1144-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details |
|
Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.
|
FDA
H-1146-2026
|
Food | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
EC Hot Links Seasoning 45.05#
Undeclared Sesame allergen
|
FDA
H-1140-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
FDA
H-1143-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details | |
|
Smoked Sausage Spice 32.86#
Undeclared Sesame allergen
|
FDA
H-1138-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
|
OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used.
|
FDA
Z-2714-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 5, 2026
|
Details |
|
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
|
FDA
Z-2696-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
|
FDA
Z-2701-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Feb 16, 2026
|
Details |
|
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
|
FDA
Z-2700-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Feb 16, 2026
|
Details |
|
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
|
FDA
Z-2697-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
|
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACEPT ACCESS INSTRUMENTS- 3VB EU/RLV0055-EU, INTRACEPT ACCESS INSTRUMENTS 2 VB/RLV0065, INTRACEPT ACCESS INSTRMNTS ADDITIONAL VB/RLV0075, INTRACEPT ACCESS INSTRMNTS ADDTL VB EU/RLV0075-EU
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.
|
FDA
Z-2694-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 22, 2026
|
Details |
|
VITEK 2 AST-N447 TEST KIT Product reference 424620
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
|
FDA
Z-2715-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 4, 2026
|
Details |
|
TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
|
FDA
Z-2716-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 8, 2026
|
Details |
|
Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
|
FDA
Z-2712-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
|
Details |
|
Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed for interstitial brachytherapy.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.
|
FDA
Z-2711-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Apr 3, 2026
|
Details |
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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.