Safety Recalls

17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,401–1,450 of 17,395

• 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

• 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

• 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

  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

• 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

• 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 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

• 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

• 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

  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

• 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

• 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

  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

• 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

• 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

• 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

• 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

• 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

• 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 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

  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 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 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

  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

  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

  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

• Vehicle Recall · May 21, 2026

  Honda (American Honda Motor Co.)

  2023 ACURA MDX, 2023 ACURA RDX, 2023 ACURA TLX, 2023 HONDA ODYSSEY, 2023 HONDA RIDGELINE, 2024 ACURA MDX, 2024 ACURA RDX, 2024 HONDA ODYSSEY, 2025 ACURA MDX, 2025 HONDA ODYSSEY, 2025 HONDA RIDGELINE

  Air bags that deploy unintentionally during a crash increase the risk of injury.

  Unclassified

• Medical Device Recall · May 21, 2026

  Windstone Medical Packaging, Inc.

  A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, 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

  Windstone Medical Packaging, Inc.

  A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, 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 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

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953 5605240 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-D

  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

  Medline Industries, LP

  Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY, Model Number: PAIN1699A

  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

• 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

  Boston Scientific Corporation

  CRE Wireguided 18-20mm 240cm

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

  Class II

• Vehicle Recall · May 21, 2026

  Chrysler (FCA US, LLC)

  2023 JEEP GRAND CHEROKEE L, 2023 JEEP GRAND CHEROKEE, 2024 JEEP GRAND CHEROKEE, 2024 JEEP GRAND CHEROKEE L, 2025 JEEP GRAND CHEROKEE L, 2025 JEEP GRAND CHEROKEE

  Delayed air bag deployment during a crash increases the risk of injury.

  Unclassified

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Pro Wireguided 6-8mm 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) LUMBAR PUNCTURE CHOICE, Model Number: DYNDH1215

  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.

  7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 The Groshong¿ NXT PICC provides short (less than 30 days) or long (greater than 30 days) term peripheral acce

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

  Class II

• Drug Recall · May 21, 2026

  Keystone Industries

  safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flavor, 1 oz. (29.6mL), Distributed by: Safco Dental Supply Co., Buffalo Grove, IL 60099, Made in USA, NDC 67239-0223-1.

  Defective container:may contain bottles with incomplete seals

  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