Safety Recalls

17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 2,951–3,000 of 17,559

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  MGC Health, Menthol- Cough Suppressant, Oral Anesthetic, Cough Drops, Honey Lemon, 30-count bag, Distributed By: Medical Group Care, LLC, 1035 Collier Center Way, STE 5, Naples, FL 34110, NDC: 83698-1

  This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.

  Class II

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  Discount Drug Mart Food Market, Cough Drops, Menthol- Cough Suppressant Anesthetic, Honey Lemon, 30-count bag, Distributed By: Drug Mart-Food Fair, Medina, Ohio, 44256, Made in China, NDC: 83698-150-3

  This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.

  Class II

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  exchange select, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Menthol Flavor, 30-count bag, Manufactured for Your Military Exchanges By: Medical Group Care, LLC, 1035 Collier Center Way, S

  This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.

  Class II

• Medical Device Recall · March 20, 2026

  Centinel Spine, Inc.

  Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical disc replacement.

  Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. VP SHUNT, Medline Kit Number/SKU CDS840193V; 2. SHY VP SHUNT CDS, Medline Kit Number/SKU CDS982389J; 3.

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Consumer Product Recall · March 19, 2026

  Specialized Bicycle Components Inc., of Morgan Hill, California

  Specialized Turbo Como SL 4.0 & 5.0 Bicycle Forks

  The bike's fork steerer tube can develop a small fatigue crack that can lead to a progressive failure of the fork, posing a fall hazard.

  Unclassified

• Consumer Product Recall · March 19, 2026

  Wagner Spray Tech Corp. of Plymouth, Minnesota

  Wagner 900 Series Power Steamers

  The attached hose can get excessively hot and the nozzle/gun can expel hot water during use and after the trigger is engaged, posing a serious burn hazard to consumers.

  Unclassified

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. RR-OMFS PACK-LF, Medline Kit Number/SKU DYNJ0045920D; 2. RR-OMFS PACK-LF, Medline Kit Number/SKU DYNJ00459

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Elekta, Inc.

  Brand Name: Leksell Vantage Arc System REF: 1053958

  Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. OPEN HEART CDS PART A, Medline Kit Number/SKU CDS840402AI; 2. OPEN HEART CDS, Medline Kit Number/SKU CDS98

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  United Orthopedic Corp.

  Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 2mm and 6mm Model/Catalog Number: 9323-5312 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument

  Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.

  Class II

• Vehicle Recall · March 19, 2026

  International Motors, LLC

  2023 IC BUS CESB, 2025 IC BUS CESB

  The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.

  Unclassified

• Medical Device Recall · March 19, 2026

  B Braun Medical Inc

  B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.

  Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

  Class I

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. CATARACT PACK, Medline Kit Number/SKU DYNJ48725A; 2. OCULAR PACK, Medline Kit Number/SKU DYNJ64138B; 3. O

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  DJO, LLC

  Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Description: 11-0494 - ICEMAN CLASSIC CUBE The IceMan CLASSIC3¿ cold therapy unit h

  Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. PLASTICS FREE FLAP, Medline Kit Number/SKU CDS983493N; 2. TLIF PACK, Medline Kit Number/SKU DYNJ02476O;

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: ANGIO PACK-LF, Medline Kit Number/SKU DYNJ0774765U

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. MAJOR NEURO PACK-LF, Medline Kit Number/SKU DYNJ0578916X; 2. ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Vehicle Recall · March 19, 2026

  Ford Motor Company

  2023 LINCOLN NAVIGATOR, 2024 LINCOLN NAUTILUS, 2024 LINCOLN NAVIGATOR, 2025 FORD EXPLORER, 2025 LINCOLN AVIATOR, 2025 LINCOLN NAUTILUS, 2025 LINCOLN NAVIGATOR

  Loss of the rearview camera image and certain driver assistance features, can reduce the driver’s ability to detect hazards, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. ZALE STEREOTACTIC CDS, Medline Kit Number/SKU CDS983173G; 2. EPISTAXIS TRAY, Medline Kit Number/SKU DYNDA3

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: EH BRONCHOSCOPY, Medline Kit Number/SKU DYNJT3270

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPINE PACK-LF, Medline Kit Number/SKU PHS719414B

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Integra LifeSciences Corp. (NeuroSciences)

  Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.

  Increased rate of out-of-specification endotoxin results.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges (961 in total), NEURO,

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  American Contract Systems Inc

  Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers ANCA80AP ANCA80AQ

  Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential risk for biohazard exposure, blood loss, infection, or air embolism.

  Class I

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. MICRODISECTOMY PACK, Medline Kit Number/SKU DYNJ80585B; 2. MICRODISECTOMY PACK, Medline Kit Number/SKU DYN

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPINAL FUSION, Medline Kit Number/SKU CDS860017AG

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Consumer Product Recall · March 19, 2026

  Tainoki Fine Furniture, of Brea, California

  Swivel Office Chairs

  The recalled chairs' base can bend, posing a fall hazard.

  Unclassified

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: GENERAL KIT, Medline Kit Number/SKU DYNJ905664I

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  B Braun Medical Inc

  B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2096A.

  Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

  Class I

• Medical Device Recall · March 19, 2026

  B Braun Medical Inc

  B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096

  Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

  Class I

• Medical Device Recall · March 19, 2026

  B Braun Medical Inc

  B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.

  Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

  Class I

• Medical Device Recall · March 19, 2026

  DJO, LLC

  Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Number: 11-1422 Software Version: no Product Description: 11-1422 - ICEMAN W/,UNIV,LOOP,NS,RH The IceMan CLASSIC3¿ cold th

  Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. ENDOSCOPY-LF, Medline Kit Number/SKU DYNJ22890M; 2. ENDOSCOPY PACK, Medline Kit Number/SKU DYNJ40645B;

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Integra LifeSciences Corp. (NeuroSciences)

  Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.

  Increased rate of out-of-specification endotoxin results.

  Class II

• Medical Device Recall · March 19, 2026

  United Orthopedic Corp.

  Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument

  Due to a design issue causing the incorrect engraved numbering on implant that could result in the incorrect orientation of the implant.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. ROBOTIC HYSTERECTOMY, Medline Kit Number/SKU DYNJ904269B; 2. ROBOTIC HYSTERECTOMY, Medline Kit Number/SKU

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Boston Scientific Corporation

  Boston Scientific Pacemaker, Implantable Pulse Generator, Pacemaker (non- Cardiac Re-Synchronization Therapy) labeled as: 1. ESSENTIO SR SL, Model Number L100; 2. ESSENTIO DR SL Pacemaker, Model

  Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps)1 and the advisory population is expanding to include all CRT-P and dual-chamber extended life (DR-EL) devices. Dual chamber modes are specifically indicated for treatment of the following: " Conduction disorders that require restoration of AV synchrony, including varying degrees of AV block " VVI intolerance (i.e., pacemaker syndrome) in the presence of persistent sinus rhythm " Low cardiac output or congestive heart failure secondary to bradycardia

  Class I

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. ANTERIOR CERVICAL FUSION PACK, Medline Kit Number/SKU DYNJ40566C; 2. OB PACK (OBSJD)642-LF, Medline Kit Num

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline and Centurion medical procedure kits, containing Medline Neuro Sponges (1229 in total), HEAD & NECK TRAY, SINUS, SMR, etc.

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  DJO, LLC

  Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Number: 11-9099 Software Version: No Product Description: 11-9099 - ICEMAN, W/COLDPAD, NS, RH The IceMan CLASSIC3¿ cold th

  Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

  Class II

• Medical Device Recall · March 19, 2026

  B Braun Medical Inc

  B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.

  Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

  Class I

• Drug Recall · March 19, 2026

  Amneal Pharmaceuticals, LLC

  traMADol Hydrochloride Tablets, USP, 50 mg, 500-count bottles, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382220, India, Distributed by: Amneal Pharmaceuticals LLC, Glasgow

  Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval during Long term stability (25¿C/60%RH).

  Class II

• Consumer Product Recall · March 19, 2026

  Dongguanshi Aokaolan Trading Co., Ltd., dba Goregent Official Store, of China

  Goregent Infant Walkers

  The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.

  Unclassified

• Medical Device Recall · March 19, 2026

  Integra LifeSciences Corp. (NeuroSciences)

  Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

  Increased rate of out-of-specification endotoxin results.

  Class II

• Medical Device Recall · March 19, 2026

  Integra LifeSciences Corp. (NeuroSciences)

  Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.

  Increased rate of out-of-specification endotoxin results.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges (1050 in total), BIOBURDEN TEST KIT, NEURO, ROBOTIC, ACDF, ENT, etc.

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. NEURO PACK, Medline kit number/SKU DYNJ64479; 2. CRANIO/NEURO/SPINE, Medline kit number/SKU DYNJ901072D.

  During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

  Class II

• Medical Device Recall · March 19, 2026

  Integra LifeSciences Corp. (NeuroSciences)

  Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.

  Increased rate of out-of-specification endotoxin results.

  Class II

• Medical Device Recall · March 19, 2026

  B Braun Medical Inc

  B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.

  Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

  Class I