Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 176 - 200 of 3,083 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Park Outside: High Voltage Battery May Catch Fire Hyundai Motor America (Hyundai) is recalling certain 2023-2024 Ioniq 5 vehicles. The high voltage battery cells may contain misaligned electrodes, which can lead to a fire while parked or driving. A fire increases the risk of injury.	NHTSA 26V432000	Vehicle	High	Jul 2, 2026 Recall: Jul 2, 2026	Details
Park Outside: Fire from Overheated Power Seat Motors Kia America, Inc. (Kia) is recalling certain 2020-2024 Telluride vehicles. The front power seat motor may overheat due to a stuck power seat slide knob or an improper recall 24V407 repair, which can result in a fire while parked or driving. A fire increases the risk of injury.	NHTSA 26V430000	Vehicle	High	Jul 2, 2026 Recall: Jul 2, 2026	Details
Parking & Daytime Running Lights May Fail/FMVSS 108 Chrysler (FCA US, LLC) is recalling certain 2026 Ram 1500 vehicles. The headlight wiring may cause the parking lights and daytime running lights to flicker on and off, or fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment." Parking lights and daytime running lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.	NHTSA 26V421000	Vehicle	High	Jul 1, 2026 Recall: Jul 1, 2026	Details
Parking & Daytime Running Lights May Fail/FMVSS 108 Chrysler (FCA US, LLC) is recalling certain MOPAR headlights with part numbers 68530384AD, 68530384AE, 68530385AD, and 68530385AE. The headlight wiring may cause the parking lights and daytime running lights to flicker on and off, or fail. As such, this equipment fails to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment." Parking lights and daytime running lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.	NHTSA 26E040000	Vehicle	High	Jul 1, 2026 Recall: Jul 1, 2026	Details
Integrated Brake System Malfunction BMW of North America, LLC (BMW) is recalling certain 2025 Mini Cooper S, Mini Countryman S All4, X2, 2024 Rolls-Royce Spectre, 2023-2025 i7, 7 Series, X7, 2024-2025 i5, 5 Series, 2023-2024 XM, X1, 2024-2025 X6, and X5 vehicles. The integrated brake (IB) system may malfunction and result in a loss of power brake assist or cause the Antilock Brake (ABS) and Dynamic Stability Control (DSC) systems to not function properly. A loss of power brake assist can extend the distance required to stop the vehicle. Additionally, malfunctioning ABS and/or DSC systems can cause a loss of vehicle control. Either of these scenarios can increase the risk of a crash.	NHTSA 26V422000	Vehicle	High	Jul 1, 2026 Recall: Jul 1, 2026	Details
Rearview Camera Image May Not Display/FMVSS 111 Honda (American Honda Motor Co.) is recalling certain 2018-2020 Odyssey vehicles. Water may enter into the rearview camera, which can cause the rearview camera image to fail to display when the vehicle is in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.	NHTSA 26V423000	Vehicle	High	Jul 1, 2026 Recall: Jul 1, 2026	Details
6/11oz Sunflower Seeds Salted The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.	FDA H-1118-2026	Food	High	Jul 1, 2026 Recall: Apr 29, 2026	Details
boichik bagles Tuna Salad Ingredients: albacore tuna, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.	FDA H-1132-2026	Food	High	Jul 1, 2026 Recall: May 22, 2026	Details
Joy Peach Lassi 16 oz. Product not adequately pasteurized	FDA H-1092-2026	Food	High	Jul 1, 2026 Recall: Apr 23, 2026	Details
Joy Salty Lassi 16 oz. Product not adequately pasteurized	FDA H-1084-2026	Food	High	Jul 1, 2026 Recall: Apr 23, 2026	Details
5# Sunflower Seeds C/NS The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.	FDA H-1122-2026	Food	High	Jul 1, 2026 Recall: Apr 29, 2026	Details
2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chips, Plastic Bag. Potential presence of Salmonella.	FDA H-1113-2026	Food	High	Jul 1, 2026 Recall: Apr 28, 2026	Details
Joy Mint Lassi 16 oz. Product not adequately pasteurized	FDA H-1091-2026	Food	High	Jul 1, 2026 Recall: Apr 23, 2026	Details
Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a yellow box, UPC 850055470040, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only). Potential Salmonella contamination.	FDA H-1102-2026	Food	High	Jul 1, 2026 Recall: Jan 9, 2026	Details
boichik bagels Whitefish Salad Ingredients: Smoked whitefish, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.	FDA H-1131-2026	Food	High	Jul 1, 2026 Recall: May 22, 2026	Details
1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a navy blue box, UPC 850055470002, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only). 2) Spring & Mulberry Pure Dark Minis Date-Sweetened Chocolate, Net Wt. 0.75 oz. (22g), individually packaged in a navy blue box, UPC 850055470132, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 64 bars (caddied)/204 bars (uncaddied) per cas Potential Salmonella contamination	FDA H-1103-2026	Food	High	Jul 1, 2026 Recall: Jan 9, 2026	Details
Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor 5500, 1.4 Ghz, ECG only, ex; Telemetry Monitor 5500 1.4 GHz FAST EX. Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to reconnect to the PIC iX central monitoring system.	FDA Z-2579-2026	Medical Device	High	Jul 1, 2026 Recall: Jun 5, 2026	Details
Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242 Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.	FDA Z-2529-2026	Medical Device	High	Jul 1, 2026 Recall: May 20, 2026	Details
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2571-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered) Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).	FDA Z-2563-2026	Medical Device	High	Jul 1, 2026 Recall: Apr 30, 2026	Details
Off-Axis Comprehensive Shoulder System Small, Augment, Off-Axis, Reamer Guide, Model/Catalog Number: 110040240 Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.	FDA Z-2527-2026	Medical Device	High	Jul 1, 2026 Recall: May 20, 2026	Details
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL Hexalobe Screw; 3070-27010 2.7mm x 10mm NL Hexalobe Screw; 3070-27011 2.7mm x 11mm NL Hexalobe Screw; 3070-27012 2.7mm x 12mm NL Hexalobe Screw; 3070-27013 2.7mm x 13mm NL Hexalobe Screw; 3070-27014 2.7mm x 14mm NL Hexalobe Screw; 3070-27015 2.7mm x 15mm NL Hexalobe Screw; 3070-27016 2.7mm x 16mm NL Hexalobe Screw; 3070-27017 2.7mm x 17mm NL Hexalobe Screw; 3070-27018 2.7mm x 18mm NL Hexalobe Screw; 3076-30010 3.0mm x 10mm NL Hexalobe Screw; 3076-30012 3.0mm x 12mm NL Hexalobe Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.	FDA Z-2532-2026	Medical Device	High	Jul 1, 2026 Recall: May 28, 2026	Details
Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444 Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.	FDA Z-2530-2026	Medical Device	High	Jul 1, 2026 Recall: May 20, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. FTMC C-SECTION TRAY-LF DYNJ54603B 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-2596-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. BARIATRIC DYNJ905153J DYNJ905153K DYNJ905153L GYNE LAPAROTOMY PACK-LF DYNJ49593A LAPAROSCOPY DYNJ905157G DYNJ905157I DYNJ905157J LAPAROSCOPY PACK DYNJ56930B MAJOR PLUS PACK DYNJ905160J DYNJ905160K DYNJ905160M MINIMALLY INVASIVE PACK-LF DYNJ0843063K PERCUTANEOUS TRAY DYNJ80196 ROBOTIC PACK DYNJ908706 DYNJ908706B 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-2583-2026	Medical Device	High	Jul 1, 2026 Recall: Feb 27, 2026	Details

Showing 176 - 200 of 3,083 product recalls

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