Safety Recalls

17,567 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 6,501–6,550 of 17,567

• Food Recall · August 26, 2025

  Country Eggs, LLC

  o Nagatoshi Large AA Brown Omega-3 1 dozen cartons o Nijiya Large AA Brown Golden Yolk 1 dozen cartons o Mizuho Large AA Brown Omega-3 Cage 1 dozen cartons o Country Eggs Large AA Brown Sunshine Yolk

  Shell egg product potentially contaminated with salmonella.

  Class I

• Food Recall · August 26, 2025

  Extract Labs, Inc.

  Sugar-free Mixed Berry Gummies Brand Name: Extract Labs Generic Name: Dietary Supplement Strength: 10mg CBD and 10mg D9 THC per gummy Dosage: 1 gummy Form: Gummy Administration: Oral Intended use

  Potential peanut protein cross-contact.

  Class II

• Food Recall · August 25, 2025

  Abdallah Incorporated

  Sea Salt Caramel Dark Miniature, Item ID: 2237 ML. Packed On (YYMMDD): 25-07-22. 5.20 lb. Box. Abdallah Candies

  Undeclared allergen (peanut, pecan).

  Class II

• Drug Recall · August 25, 2025

  AvKARE

  chloroproMAZINE Hydrochloride Tablets, USP, 50 mg, 50 Tablets (5x10) unit dose carton, Rx only, Manufactured for: AvKare, Pulaski, TN, 38478, NDC 50268-164-15

  Presence of a foreign substance.

  Class II

• Drug Recall · August 25, 2025

  Consumer Product Partners, LLC

  TopCare Health 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC: 36800-589-14

  Cross Contamination with Other Products.

  Class III

• Drug Recall · August 25, 2025

  Consumer Product Partners, LLC

  Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC: 30142-810-14

  Cross Contamination with Other Products.

  Class III

• Drug Recall · August 25, 2025

  AvKARE

  chloroproMAZINE Hydrochloride Tablets, USP, 100 mg, 50 Tablets (5x10) unit dose carton, Rx only, Manufactured for: AvKare, Pulaski, TN, 38478, NDC 50268-165-15

  Presence of a foreign substance.

  Class II

• Medical Device Recall · August 25, 2025

  LeMaitre Vascular, Inc.

  Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft is intended to serve as a substitute conduit for blood where bypass or repla

  Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.

  Class II

• Vehicle Recall · August 25, 2025

  Kia America, Inc.

  2025 KIA K4, 2025 KIA SORENTO

  A loss of drive power increases the risk of a crash.

  Unclassified

• Food Recall · August 25, 2025

  Abdallah Incorporated

  Cream Caramels, Milk, Item ID: 2210L. Packed On (YYMMDD): 25-06-16. 6.26 lb. Box. Abdallah Candies

  Undeclared allergen (peanut, pecan).

  Class II

• Medical Device Recall · August 22, 2025

  Sonesta Medical AB

  Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software Version: N/A Product Description: Sonesta 6210 - Procedure table designed for full fluoroscopic imaging of the u

  Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.

  Class II

• Medical Device Recall · August 22, 2025

  CooperVision, Inc.

  Voyant 1-Day Premium Toric, (stenfilcon A) contact lens. Model Number: Voyant 1-Day Premium Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Dai

  One lot manufactured with an invalid sterilization cycle.

  Class II

• Medical Device Recall · August 22, 2025

  CooperVision, Inc.

  Sofmed Breathables, (stenfilcon A) contact lens. Model Number: Softmed Breathables. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable W

  One lot manufactured with an invalid sterilization cycle.

  Class II

• Vehicle Recall · August 22, 2025

  Forest River, Inc.

  2024 EAST TO WEST ENTRADA

  Trailer brake lockup increases the risk of a crash.

  Unclassified

• Vehicle Recall · August 22, 2025

  Ford Motor Company

  2024 FORD MUSTANG, 2025 FORD MUSTANG

  License plate, side marker, and tail lights that fail to illuminate as intended can reduce visibility to other drivers, increasing the risk of a crash.

  Unclassified

• Vehicle Recall · August 22, 2025

  Ford Motor Company

  2025 FORD EXPLORER, 2025 LINCOLN AVIATOR

  Trailer tail lights that do not illuminate as intended can reduce visibility to other drivers, increasing the risk of a crash.

  Unclassified

• Vehicle Recall · August 22, 2025

  Ford Motor Company

  2025 FORD F-450 SD, 2026 FORD F-550 SD, 2026 FORD F-350 SD, 2026 FORD F-450 SD

  An instrument panel display that does not show critical information, such as warning lights or vehicle speed, increases the risk of a crash.

  Unclassified

• Medical Device Recall · August 22, 2025

  CooperVision, Inc.

  MyDay Toric, stenfilcon A) Contact Lens. Model/Catalog Number: MyDay Toric. 54% water content, Toric, cast moulded Silicone Hydrogel, In-monomer tinted, contact lens, for Daily Disposable Wear. Bli

  One lot manufactured with an invalid sterilization cycle.

  Class II

• Medical Device Recall · August 22, 2025

  GE Medical Systems, LLC

  MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4

  If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the Acquisition Trunk Cable. This is visible as a damaged sheath or exposed wires. If a damaged Acquisition Trunk Cable is not recognized and removed from service, the cable can overheat with continued use.

  Class II

• Drug Recall · August 22, 2025

  GRACE & FIRE PTY LTD

  Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF 50 Blurring Mineral SkinScreen, Zinc Oxide 22.75%, 15 mL, 0.5 fl. oz. per tube, Supreme Sunscreen SPF 50, 15 mL 0.5 fl. oz. per tube, Dis

  Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.

  Class II

• Vehicle Recall · August 22, 2025

  New Flyer of America, Inc.

  2025 NEW FLYER XCELSIOR

  An insufficient number, or incorrectly located, of emergency exits can prevent or delay passengers from exiting during an emergency, increasing their risk of injury.

  Unclassified

• Drug Recall · August 22, 2025

  GRACE & FIRE PTY LTD

  Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, Zinc Oxide 22.75%, a) 15 mL, 0.5 fl. oz. per tube, NDC 84803-106-01, UPC 9355909006068, b) 50 mL, 1.7 fl. oz. per tube, NDC 84803-106

  Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.

  Class II

• Vehicle Recall · August 22, 2025

  Forest River, Inc.

  2026 FOREST RIVER FLAGSTAFF, 2026 FOREST RIVER ROCKWOOD

  An inoperative breakaway switch increases the risk of a crash.

  Unclassified

• Food Recall · August 21, 2025

  Taylor Farms Retail, Inc.

  Salad Kit labeled as follows: Taylor FARMS Honey Balsamic SALAD KIT, NET WT. 8.3 OZ (235g), INGREDIENTS: HONEY BALSAMIC VINAIGRETTE (soybean oil ...) SPINACH, CARROT, SEA SALT CROISSANT CROUTON (wheat

  Undeclared allergens (sesame and soy).

  Class I

• Medical Device Recall · August 21, 2025

  Folsom Metal Products, Inc.

  Frontier Devices, REF: 301.914S2, 14 mm Distraction Pin, 10 double packs , Rx Only, Sterile

  Labeling includes shelf life that has not been validated.

  Class II

• Medical Device Recall · August 21, 2025

  Abbott Point Of Care Inc.

  i-STAT EG7+ cartridge. List Number: 03P76-25.

  Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.

  Class II

• Medical Device Recall · August 21, 2025

  Folsom Metal Products, Inc.

  Frontier Devices, REF: 301.916S1, 16 mm Distraction Pin, 10 single packs , Rx Only, Sterile

  Labeling includes shelf life that has not been validated.

  Class II

• Medical Device Recall · August 21, 2025

  Abbott Point Of Care Inc.

  i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914, K940918, K223710, K230275, K230285, K230300

  Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.

  Class II

• Medical Device Recall · August 21, 2025

  Medline Industries, LP

  Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q

  The kits contain certain lots of cannula products where the catheter may not retain its shape.

  Class I

• Medical Device Recall · August 21, 2025

  Folsom Metal Products, Inc.

  Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile

  Labeling includes shelf life that has not been validated.

  Class II

• Medical Device Recall · August 21, 2025

  Folsom Metal Products, Inc.

  Frontier Devices, REF: 301.912S1, 12 mm Distraction Pin, 10 single packs , Rx Only, Sterile

  Labeling includes shelf life that has not been validated.

  Class II

• Vehicle Recall · August 21, 2025

  International Motors, LLC

  2026 INTERNATIONAL MV

  A short circuit increases the risk of a fire.

  Unclassified

• Medical Device Recall · August 21, 2025

  Abbott Point Of Care Inc.

  i-STAT EG6+ cartridge. List Number: 03P77-25.

  Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.

  Class II

• Medical Device Recall · August 21, 2025

  Folsom Metal Products, Inc.

  Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 5 single packs , Rx Only, Sterile

  Labeling includes shelf life that has not been validated.

  Class II

• Vehicle Recall · August 21, 2025

  Aluminum Trailer Company (ATC)

  2023 ATC PL700, 2024 ATC RM900

  Overheated radio and speakers increase the risk of a fire.

  Unclassified

• Medical Device Recall · August 21, 2025

  Abbott Point Of Care Inc.

  i-STAT CG4+ cartridge (white). List Number: 03P85-25.

  Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to reflect updated sample type for lactate and measurement ranges for pH and PO2.

  Class II

• Vehicle Recall · August 21, 2025

  General Motors, LLC

  2023 CHEVROLET CORVETTE, 2024 CHEVROLET CORVETTE

  A fuel leak in the presence of an ignition source, such as hot engine or exhaust components, can increase the risk of a fire.

  Unclassified

• Food Recall · August 21, 2025

  Latitude 36 Foods

  Honey Balsamic dressing, 3.4 ounce plastic pouch, Best by date and Lot number appear directly on pouch.

  Product contains undeclared Soy and Sesame

  Class I

• Food Recall · August 21, 2025

  Blue Bell Creameries, L.P.

  Chocolate Chip Cookie Dough ice cream cartons with a Moo-llennium Crunch lid. Packaging contains Moo-llennium crunch. Packaged in half gallon cartons (1.89 L)

  undeclared almond, walnut, and pecan.

  Class II

• Medical Device Recall · August 21, 2025

  Bard Peripheral Vascular Inc

  Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to identify internal wiring anomalies in the Venclose EVSRF Ablation Catheter prior to use. The Venclose digiRF Generator is a sop

  Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in Venclose EVSRF Ablation Catheters prior to clinical use. This automated diagnostic check is executed immediately upon catheter connection to the generator, occurring before the procedure interface becomes accessible. When a catheter fails this verification process, the generator displays a Red X indicator on the screen without accompanying error codes, effectively disabling catheter functionality. However, BD has determined that software version 3.35 generates false positive failures due to temperature-dependent verification parameters, incorrectly flagging properly functioning Venclose EVSRF Ablation Catheters as defective when the catheter temperature is not at steady state during the check initiation.

  Class II

• Vehicle Recall · August 21, 2025

  Rivian Automotive, LLC

  2025 RIVIAN R1T, 2025 RIVIAN R1S

  A loss of drive power increases the risk of a crash.

  Unclassified

• Medical Device Recall · August 21, 2025

  Folsom Metal Products, Inc.

  Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 10 single packs , Rx Only, Sterile

  Labeling includes shelf life that has not been validated.

  Class II

• Consumer Product Recall · August 21, 2025

  IBC Technologies USA Inc., of Lawnside, New Jersey

  CX Series Combi Boiler

  A combi (or combination) boiler is a type of gas boiler that provides both a home's hot water and central heating. The hot water can exceed the temperature set on the control panel, posing a burn hazard to users.

  Unclassified

• Food Recall · August 20, 2025

  The J.M. Smucker Company

  Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7 oz) UPC 8 88109 11061 1; 16-1.28 oz carton (20.31 oz) Individual selling unit - UPC

  Mold. The firm noticed an increase in customer complaints. They conducted a root cause investigation and discovered that one of their coolers had malfunctioning.

  Class II

• Medical Device Recall · August 20, 2025

  Boston Scientific Corporation

  Model Number L111, ESSENTIO DR SL MRI Pacemaker

  Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

  Class I

• Medical Device Recall · August 20, 2025

  Boston Scientific Corporation

  Model Number U226, VISIONIST CRT-P EL

  Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

  Class I

• Medical Device Recall · August 20, 2025

  Boston Scientific Corporation

  ACCOLADE SR SL MRI (Model L310)

  Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

  Class I

• Medical Device Recall · August 20, 2025

  Boston Scientific Corporation

  PROPONENT SR SL (Model L200)

  Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

  Class I

• Medical Device Recall · August 20, 2025

  Boston Scientific Corporation

  PROPONENT DR SL (Model L201)

  Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

  Class I

• Medical Device Recall · August 20, 2025

  Boston Scientific Corporation

  Model Number L221 PROPONENT DR EL Pacemaker

  Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

  Class I