Safety Recalls

17,553 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,551–1,600 of 17,553

• Vehicle Recall · May 27, 2026

  Toyota Motor Engineering & Manufacturing

  2024 TOYOTA LAND CRUISER HYBRID

  An instrument panel display that fails to show critical safety information, such as engine coolant temperature or electrical charge increases the risk of a crash or injury.

  Unclassified

• Drug Recall · May 27, 2026

  Lannett Company Inc.

  Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 62175-322-46.

  Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.

  Class II

• Medical Device Recall · May 27, 2026

  Inter-Med Llc

  Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28

  Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.

  Class II

• Vehicle Recall · May 27, 2026

  Ford Motor Company

  2023 FORD BRONCO SPORT, 2023 FORD MAVERICK, 2024 FORD BRONCO SPORT, 2024 FORD MAVERICK

  A detached control arm can cause a loss of vehicle control, increasing the risk of a crash.

  Unclassified

• Food Recall · May 27, 2026

  Produce Innovations

  Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green adhesive label. The label reads in part as "***Lunch Box Kitchen*** Premium Convenience***Turkey & Cheddar Sub***B

  Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich

  Class III

• Vehicle Recall · May 27, 2026

  Ford Motor Company

  2025 FORD EXPLORER

  A sudden loss of drive power can increase the risk of a crash.

  Unclassified

• Vehicle Recall · May 27, 2026

  Tiffin Motorhomes, Inc.

  2026 TIFFIN OPEN TRAIL, 2026 TIFFIN WAYFARER

  The incorrect label color may make it difficult for the operator to locate the loading or tire pressure information, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · May 27, 2026

  Medtronic MiniMed, Inc.

  MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896

  A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).

  Class II

• Vehicle Recall · May 26, 2026

  Alliance RV, LLC

  2026 ALLIANCE RV PARADIGM

  Broken shock retainer bolt heads and washers may detach and become a road hazard to other vehicles, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · May 26, 2026

  Philips North America Llc

  Philips Avalon Fetal Monitor, FM 30 Part numberM2703A

  Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

  Class II

• Medical Device Recall · May 26, 2026

  Philips North America Llc

  Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A

  Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

  Class II

• Vehicle Recall · May 26, 2026

  Forest River, Inc.

  2024 FOREST RIVER R-POD

  Broken shock retainer bolt heads and washers may detach and become a road hazard for other vehicles, increasing the risk of a crash.

  Unclassified

• Food Recall · May 26, 2026

  Nutricia North America

  functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2

  Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

  Class II

• Food Recall · May 26, 2026

  Nutricia North America

  functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY COMPLETE PLANT BASED NUTRITION NET WT. 12 OZ (341g) case UPC 8 57858 00445 8, package UPC 8 57858 00447

  Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.

  Class II

• Medical Device Recall · May 25, 2026

  Medtronic Perfusion Systems

  Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula

  Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

  Class II

• Medical Device Recall · May 25, 2026

  Medtronic Perfusion Systems

  Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula

  Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

  Class II

• Food Recall · May 24, 2026

  MOGO Moringa LLC

  MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Po

  Product may be contaminated with Salmonella Typhimurium

  Class I

• Food Recall · May 23, 2026

  Bazzini LLC

  Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.

  Undeclared peanuts

  Class I

• Medical Device Recall · May 22, 2026

  Abiomed, Inc.

  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.

  Class I

• Medical Device Recall · May 22, 2026

  Abiomed, Inc.

  Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13 and 25 cm Japan. Product Code: 1000542.

  Potential for thrombus formation during prolonged use of the introducer.

  Class I

• Medical Device Recall · May 22, 2026

  Abiomed, Inc.

  Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435.

  Potential for thrombus formation during prolonged use of the introducer.

  Class I

• Medical Device Recall · May 22, 2026

  W L Gore & Associates, Inc.

  GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1010. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common bile duct which may be obstructed.

  10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).

  Class II

• Medical Device Recall · May 22, 2026

  Hamilton Medical AG

  IntelliCuff, Portable automatic cuff pressure controller REF: 951001

  Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.

  Class II

• Medical Device Recall · May 22, 2026

  W L Gore & Associates, Inc.

  GORE VIABIL Short Wire Biliary Endoprosthesis, Model No. VSWVN1006. Flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common bile duct which may be obstructed.

  10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).

  Class II

• Food Recall · May 22, 2026

  University of California Health Milk Bank

  001165: Standard Pasteurized Donor Human Milk; 100 mL bottles 001198: Pediatric Pasteurized Donor Human Milk; 200 mL bottles No UPC

  Product is potentially contaminated with foreign material (plastic particles).

  Class II

• Medical Device Recall · May 22, 2026

  Innovasis, Inc

  Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System

  Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque instrument with undersized condition which could prevent mating tip from engaging with the pedicle screw tulip and rod during tightening, which may lead to surgical delay, intervention/alternative methods to perform final tightening step.

  Class II

• Medical Device Recall · May 22, 2026

  Medtronic Heart Valves Division

  Medtronic Harmony Delivery Catheter System

  Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a manufacturing issue.

  Class I

• Vehicle Recall · May 22, 2026

  Brinkley RV

  2025 BRINKLEY RV MODEL Z, 2026 BRINKLEY RV MODEL Z

  Broken shock retainer bolt heads and washers may detach and become a road hazard for other vehicles, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · May 22, 2026

  Abiomed, Inc.

  Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834.

  Potential for thrombus formation during prolonged use of the introducer.

  Class I

• Drug Recall · May 22, 2026

  Zep Inc

  Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-1

  Microbial contamination of sterile products

  Class II

• Food Recall · May 22, 2026

  Boichik Bagels, Inc.

  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

  Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.

  Class II

• Food Recall · May 22, 2026

  Boichik Bagels, Inc.

  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,

  Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.

  Class II

• Food Recall · May 22, 2026

  Total Nutrition Inc

  1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules)

  Product may be contaminated with Salmonella.

  Class I

• Food Recall · May 22, 2026

  Boichik Bagels, Inc.

  boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels NET WT 26.5 OZ (1.66 LB) 750g Ingredients: Organic wheat flour ... Contains Wheat Topped flavors may additionally contain ... sesame seed

  Undeclared allergen, sesame.

  Class II

• Drug Recall · May 22, 2026

  SUN PHARMACEUTICAL INDUSTRIES INC

  Xyvona (levorphanol tartrate tablets), 2mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV

  Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona

  Class II

• Drug Recall · May 22, 2026

  SUN PHARMACEUTICAL INDUSTRIES INC

  Xyvona (levorphanol tartrate tablets), 3mg, 100 Tablets, Rx only, Forte BioPharma, Manufactured by: Ohm Laboratories Inc., New Brunswick, NJ 08901, Distributed by: Fort Bio-Pharma, LLC., Las Vegas, NV

  Labeling: Not Elsewhere Classified. This recall has been initiated in response to the denial by FDA of marketing the product under the proprietary name Xyvona

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI Code: 0110885403108365 TPT1000 THORACENTESIS/PARACENTESIS TRAY UDI-DI Co

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Windstone Medical Packaging, Inc.

  A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit

  Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

  Class I

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Wireguided 10-12mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 The intended use of the Short-Term Dialysis Catheter is attaining temporary/short-term (less t

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Food Recall · May 21, 2026

  Alb-USA Enterprises Inc

  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 5304000050

  Undeclared colors (FD&C Yellow 5 and FD&C Red 40).

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) PAIN MGMT/ PREF W. MED NDL, Model Number: PAIN0072L; 2) CONTINUOUS EPIDURAL TRAY, Model Number: PAIN1317; 3) CONTINUOUS EPIDURAL TRAY, Model Number: PAIN1579A; 4) CSE T

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) MULTIMED, 7FR, 20CM, 3L, CVC BUNDLE, Model Number: ECVC5995; 2) TRIPLE LUMEN CENTRAL LINE BUNDLE, Model Number: ECVC2625; 3) INTROFLEX 6F, 1L, TB, US, Model Number: S

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129278 P4254108D PowerMidline Catheter 4 Fr Dual

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Pro Wireguided 12-15mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Drug Recall · May 21, 2026

  Keystone Industries

  DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Manufactured for and Distributed by Dental Health Products, Inc, 2614 North Sugar Bush Road, New Franken, WI 54229. NDC 696

  Defective container:may contain bottles with incomplete seals

  Class II

• Vehicle Recall · May 21, 2026

  Chrysler (FCA US, LLC)

  2023 CHRYSLER PACIFICA

  A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129 CK000883 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188800 CK000884A PowerPICC Proven

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Wireguided 18-20mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO, Model Number: DYNJ57922A

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II