Safety Recalls

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

Showing 2,251–2,300 of 17,553

• Medical Device Recall · April 27, 2026

  Oculus Technologies of Mexico, S.A. de C.V.

  PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

  The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.

  Class II

• Medical Device Recall · April 27, 2026

  Becton Dickinson & Company

  BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 40574

  This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

  Class I

• Medical Device Recall · April 27, 2026

  Becton Dickinson & Company

  BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.

  This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

  Class I

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A CVC/PICC/MIDLINE DRESSING CHANGE KIT EBSI1057A DIALYSIS DRESSING CHANGE EBSI1498 EBSI CVC DRESSING CHANGE KIT E

  Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

  Class II

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kits: DAVINCI MAIN DYNJ908031D

  Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

  Class II

• Drug Recall · April 27, 2026

  Ascend Laboratories, LLC

  Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ

  Failed Dissolution Specifications

  Class II

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kits: ACD DYNJ904999J ACDF DYNJ907336B DYNJ910821A ACDF PACK DYNJ81098C ACL DYNJ911996 ACL ACCESSORY PACK DYNJ86584B ACL- LF DYNJ905281B ACL PACK DYNJ6

  Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

  Class II

• Medical Device Recall · April 27, 2026

  Becton Dickinson & Company

  BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.

  This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.

  Class I

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A

  Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

  Class II

• Food Recall · April 27, 2026

  Sugar Foods LLC

  Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202

  Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.

  Class I

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kit: SMSC-PELVISCOPY PACK-LF DYNJ0161619M

  Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

  Class II

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kit: HERNIA REPAIR TOTE DYNJ908337D

  Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

  Class II

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 10lbs (4.54kg) Ingredients: *** nonfat dry milk *** GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 30LB (13.61kg

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX MOCHA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UP

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.41kg Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620386

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PREMIUM HOT COCOA MIX NET WT 32oz (2lbs) 907g Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620126

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX CLASSIC WHITE NET WT 10lbs (4.54kg)

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA NET WT 48oz (3lbs) 1.36kg Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620232

  Potential contamination with Salmonella.

  Class I

• Food Recall · April 26, 2026

  Ghirardelli Chocolate Company

  GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX VANILLA NET WT 48oz (3lbs) 1.36kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 74759

  Potential contamination with Salmonella.

  Class I

• Drug Recall · April 24, 2026

  Lannett Company Inc.

  Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1231-01.

  Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.

  Class III

• Medical Device Recall · April 24, 2026

  GE Medical Systems Information Technologies Inc

  GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With

  GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

  Class II

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6036786 Instant Country Gravy Seasoning, 40lb bag

  potential to be contaminated with Salmonella

  Class I

• Medical Device Recall · April 24, 2026

  Bayer Medical Care, Inc.

  Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629

  Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.

  Class II

• Medical Device Recall · April 24, 2026

  Medartis AG

  Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation

  The cannulation of the CCS screw is not centered.

  Class II

• Medical Device Recall · April 24, 2026

  GE Medical Systems Information Technologies Inc

  CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3

  Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charring or discoloration of thermal printer paper. Ignition of the paper could potentially result in serious thermal injury.

  Class II

• Food Recall · April 24, 2026

  Target Corporation

  Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. DPCI # 878-02-0227. UPC (01) 00250086000009 (3922) 00999. Distributed by Super

  Undeclared allergens (sesame and soy)

  Class II

• Medical Device Recall · April 24, 2026

  GE Medical Systems Information Technologies Inc

  GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Pati

  GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

  Class II

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6035415 Sourdough Cheese Crouton Seasoning, 50lb bag

  potential to be contaminated with Salmonella

  Class I

• Medical Device Recall · April 24, 2026

  GE Medical Systems Information Technologies Inc

  GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia D

  GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

  Class II

• Medical Device Recall · April 24, 2026

  BERLIN HEART GMBH

  EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01

  Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.

  Class II

• Vehicle Recall · April 24, 2026

  Volkswagen Group of America, Inc.

  2025 AUDI Q5, 2025 AUDI SQ5

  Improperly restrained occupants have an increased risk of injury during a crash.

  Unclassified

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6036195 Ranch Seasoning, 50lb bag

  potential to be contaminated with Salmonella

  Class I

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6035687 Bayou Blackened Ranch Seasoning, 25lb bag

  potential to be contaminated with Salmonella

  Class I

• Medical Device Recall · April 24, 2026

  GE Medical Systems Information Technologies Inc

  GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patien

  GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

  Class II

• Medical Device Recall · April 24, 2026

  GE Medical Systems Information Technologies Inc

  GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection

  GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

  Class II

• Food Recall · April 24, 2026

  Solina U.S. Holding

  YT 6027393 Spicy Ranch Blend, 50lb bag

  potential to be contaminated with Salmonella

  Class I

• Medical Device Recall · April 24, 2026

  Devicor Medical Products Inc

  HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3

  Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.

  Class II

• Drug Recall · April 24, 2026

  Lupin Pharmaceuticals Inc.

  Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur 441108, INDIA, a) 2 Pens- NDC 70748-346-02

  Presence of particulate matter: a white thread-like structure in the cartridge

  Class II

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6036277 Garlic Cream Sauce Seasoning, 40lb bag

  potential to be contaminated with Salmonella

  Class I

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6036443 Cheddar Cheese Powder Seasoning, 50lb bag

  potential to be contaminated with Salmonella

  Class I

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6036087 Cr¿me Fraiche Spice Seasoning, 25lb bag

  potential to be contaminated with Salmonella

  Class I

• Medical Device Recall · April 24, 2026

  GE Medical Systems Information Technologies Inc

  GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physio

  GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).

  Class II

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6036554 Parmesan Breadstick Sauce Seasoning, 40lb bag

  potential to be contaminated with Salmonella

  Class I

• Drug Recall · April 24, 2026

  Wisconsin Pharmacal Company

  MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), Manufactured by: Pharmacal 1 Pharmacal Way, P.O. Box 198, Jackson, WI 53037.

  Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.

  Class I

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6022487 Garlic Herb Topping, 50lb bag

  potential to be contaminated with Salmonella

  Class I

• Drug Recall · April 24, 2026

  Teva Pharmaceuticals USA, Inc

  Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Single-Dose kits containing: 8-mL vial of 30 mg strength, a pre-filled syringe containing 2 mL of diluent, one vi

  Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

  Class II

• Medical Device Recall · April 24, 2026

  Intuitive Surgical, Inc.

  Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product Description: Preface: This report under 21 CFR 806.10 is being submitted for

  Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the handheld camera to the robotic endoscope.

  Class II