Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent Product Recall Alerts List
Showing 1,676 - 1,700 of 4,975 matching product recalls.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
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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.
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NHTSA
26V457000
|
Vehicle | Unknown |
Jul 16, 2026
Recall: Jul 16, 2026
|
Details |
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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.
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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 | |
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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.
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FDA
H-1148-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 25, 2026
|
Details |
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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.
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FDA
H-1150-2026
|
Food | High |
Jul 15, 2026
Recall: Jun 24, 2026
|
Details |
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JB Chicken Sknls 35.73#
Undeclared Sesame allergen
|
FDA
H-1139-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
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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 |
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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 |
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FDA
H-1145-2026
|
Food | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details | |
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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 | |
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Smoked Sausage Spice 32.86#
Undeclared Sesame allergen
|
FDA
H-1138-2026
|
Food | High |
Jul 15, 2026
Recall: May 7, 2026
|
Details |
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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.
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FDA
Z-2714-2026
|
Medical Device | High |
Jul 15, 2026
Recall: Jun 5, 2026
|
Details |
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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 |
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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 |
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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.
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FDA
Z-2697-2026
|
Medical Device | High |
Jul 15, 2026
Recall: May 28, 2026
|
Details |
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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 |
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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.
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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.
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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 |
Recent Product Recall Alerts
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Latest Product Recalls FAQ
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