Safety Recalls

15,182 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 801–850 of 15,182

• Medical Device Recall · April 27, 2026

  Windstone Medical Packaging, Inc.

  Aligned Medical AMS16835 Fluids Kit RX

  Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.

  Class II

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kits: BIB AV FISTULA PACK DYNJ58304B CARDIAC MINOR SURGICOUNT PACK DYNJ56573B ENDOVASCULAR PACK DYNJ29135N EP DEVICE DYNJ65916B FULL LINE ANEURYSM CDS CDS983672

  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: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C

  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 EBSI Kit EBSI1534

  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: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C

  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

  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

  Medline Industries, LP

  Medline convenience kit: IV START KIT W/HUBGUARD DYNDV2662

  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

  Golden State Medical Supply Inc.

  Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01

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

  Class III

• Drug Recall · April 27, 2026

  Golden State Medical Supply Inc.

  Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05

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

  Class III

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B

  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 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.

  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: BREAST-HERNIA-PORT CDS-LF CDS984853L

  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: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C PACEMAKER PK DYNJT3454 PACEMAKER/ICD PACK DYNJ33822L PAD OPEN HEART DYNJ900962O PED

  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: PORT A CATH DYNJ906818A

  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: 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

• 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: DISCECTOMY PACK DYNJ86476B EAR DYNJ81460C DYNJ900004J DYNJ901779J DYNJ902900F EAR PACK DYNJ81419D ENT PACK DYNJ40498B HEAD & NECK CDS DYNJ901246J JE

  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: 20CM CVC INSERTION KIT ECVC6805B 2L 8.5FR 16CM CVC INSERTION KIT ECVC8055A VANTEX PI CVC 7F, 3L, 20CM BUNDLE ECVC6915A ECVC6985B

  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

  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

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kit: BHS NEURO DYNJ904900N MEDTRX NEURO PACK DYNJ67267B MRI DBS PACK DYNJ9814630O NEURO CDS-LF CDS983383L NEURO PACK DYNJ59397Q DYNJT7315 NEURO PACK-LF DYN

  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: KIT: DRESSING CHANGE PED DYNDC3359

  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

  MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G

  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 Number: 405671.

  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

• Drug Recall · April 27, 2026

  Oasis Medical, Inc.

  Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Manufactured for: OASIS Medical, Inc., 514 S. Vermont Ave., Glendora, CA 91741, USA, Made in France, NDC 42126-6

  Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.

  Class II

• Medical Device Recall · April 27, 2026

  Medline Industries, LP

  Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS98237

  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: BASIC EYE DYNJ905154I TUBAL LIGATION CDS CDS760053K

  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

  The Brownie Baker Inc.

  cafe nouria blueberry muffin NET WT. 6 OZ (170g) UPC: 811070033986

  Undeclared walnuts

  Class II

• 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 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 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 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 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 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 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 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 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

• 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 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

• 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

• 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

• 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

• 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

  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

• 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

• 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 6035687 Bayou Blackened Ranch Seasoning, 25lb bag

  potential to be contaminated with Salmonella

  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

• Food Recall · April 24, 2026

  Solina U.S. Holding

  Solina 6036195 Ranch Seasoning, 50lb bag

  potential to be contaminated with Salmonella

  Class I

• 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