Safety Recalls

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

Showing 2,901–2,950 of 17,559

• Food Recall · March 24, 2026

  Falcon Trading Co., Inc.

  SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI NET WT. 25 LBS. ORIGEN: ARGENTINA EXPORTADOR: ESPAR SRL FECHA PRODUCCION: 11/13/2023 Item: 003040 UPC: 086700930403

  Potential contamination with pesticides, haloxyfop and thiamethoxam

  Class III

• Vehicle Recall · March 24, 2026

  Nova Bus (US) Inc.

  2023 NOVA BUS LFS

  Failure of the tension-reliving device may prevent the seat belt from properly restraining the driver, increasing the risk of injury during a crash.

  Unclassified

• Drug Recall · March 24, 2026

  The Harvard Drug Group LLC

  Memantine Hydrochloride Extended-Release, Capsules, 7 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-6734-61

  Failed Dissolution Specifications

  Class II

• Medical Device Recall · March 24, 2026

  Medline Industries, LP

  Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038402; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.

  Medline has identified the presence of particulate within the fluid path of the Manifolds.

  Class I

• Drug Recall · March 24, 2026

  GE Healthcare Ireland Limited

  GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%), Rx Only, Distributed by: GE Healthcare Inc., Marlborough, MA 01752 USA, NDC 0407-1413-63.

  Presence of particulate matter

  Class II

• Medical Device Recall · March 24, 2026

  ICU Medical, Inc.

  Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL3960

  Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs during therapy this may result in therapy interruption with the potential for the patient to receive less infusion solution than intended. Exposure of hazardous substances to the patient, caregiver, or pharmacy technician is possible.

  Class II

• Medical Device Recall · March 24, 2026

  Foundation Medicine, Inc.

  Protocol Configuration Tool (PCT) software v1.3.0 for Hamilton AutoLys STAR used within FoundationOneCDx (F1CDx) installed on Research Triangle Park laboratory Equipment IDs 01342, 01591, 01989, 01990

  Potential for spontaneous closures of Hamilton HxRunControl software during execution of Autolys protocols after deployment of the PCT software for AutoLys Hamilton STAR.

  Class II

• Medical Device Recall · March 24, 2026

  Medline Industries, LP

  Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. MTS,RT,HANDED/LFT,HRT,KIT, Medline Kit Number/SKU 60010508; 2. DBD-MTS,LEFT HEART,KIT, Medline Kit Number/SKU 60160075;

  Medline has identified the presence of particulate within the fluid path of the Manifolds.

  Class I

• Medical Device Recall · March 24, 2026

  Medline Industries, LP

  Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO K

  Medline has identified the presence of particulate within the fluid path of the Manifolds.

  Class I

• Food Recall · March 24, 2026

  Falcon Trading Co., Inc.

  SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI NET WT. 15 LBS Item: 003056 UPC: 086700030561

  Potential contamination with pesticides, haloxyfop and thiamethoxam

  Class III

• Medical Device Recall · March 24, 2026

  Remel, Inc

  Yeastone Broth, 11ML, 10/BOX YY3462

  Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.

  Class II

• Medical Device Recall · March 24, 2026

  Medline Industries, LP

  Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B

  Medline has identified the presence of particulate within the fluid path of the Manifolds.

  Class I

• Medical Device Recall · March 24, 2026

  Medline Industries, LP

  Medline medical convenience kits, containing Namic Manifold, Labeled as: TAVI, Medline Kit Number/SKU DYNJ904981C

  Medline has identified the presence of particulate within the fluid path of the Manifolds.

  Class I

• Food Recall · March 24, 2026

  Unistel Industries Inc.

  SALUTE SEASONINGS; Ground All Spice; Net Wt 16oz; Unistel Industries 650 Blossom Road Rochester, NY 14610; UPC: 7 69203 01617 0

  Product may be contaminated with Salmonella.

  Class I

• Food Recall · March 24, 2026

  Tops Markets LLC

  Christopher Ranch Peeled Garlic 6 oz.

  The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm

  Class III

• Medical Device Recall · March 23, 2026

  Olympus Corporation of the Americas

  Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 25cm. Model Number: TB2-0525FC.

  Potential for detachment of a distal tip component of the device during use.

  Class II

• Medical Device Recall · March 23, 2026

  Advanced Bionics, LLC

  Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110; CI-5501-120; CI-5501-130; CI-5501-140; CI-5501-150; CI-5501-190; CI-5501-240; CI-550

  The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the button/coin cell battery.

  Class II

• Medical Device Recall · March 23, 2026

  Gentuity, LLC

  Gentuity HF-OCT Imaging System Model G10-01; Software version 23.2.13;

  The potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx and Vis-Rx Prime catheters. This correction is intended to ensure that users are fully informed of how to recognize, avoid, and mitigate this condition to maintain accurate longitudinal (length) measurements during OCT imaging.

  Class II

• Medical Device Recall · March 23, 2026

  THERANICA BIOELECTRONICS LTD

  Nerivio Infinity. Model/Catalog Number: FGD000100. Software Version: FW Version 4.1.2.0, App version 7.28.0.11

  Potential for the batter to have a thermal-runway event during charging, resulting in smoke and odor.

  Class II

• Medical Device Recall · March 23, 2026

  TANGENT ENDOSCOPY, LLC

  Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.

  Affected devices exhibited fractures at the distal shaft tip without complete detachment.

  Class II

• Medical Device Recall · March 23, 2026

  Olympus Corporation of the Americas

  Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 20cm. Model Number: TB2-0520FC.

  Potential for detachment of a distal tip component of the device during use.

  Class II

• Medical Device Recall · March 23, 2026

  Olympus Corporation of the Americas

  Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 45cm. Model Number: TB2-0545FC.

  Potential for detachment of a distal tip component of the device during use.

  Class II

• Medical Device Recall · March 23, 2026

  Hologic, Inc

  Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) Model/Catalog Number: CMP-01669 Software Version: N/A - not software version specific Component: Yes

  It was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the manufacturer-installed settings. Modifications included disabling Barco Application Appearance Manager (AAM), altering calibration and compliance parameters, and adjusting additional display-related settings. This field correction is being conducted to restore affected system to the validated configuration and reinforce proper use in accordance with the Operator's Manual.

  Class II

• Food Recall · March 23, 2026

  Booey's Gourmet LLC

  Booey's Dragon's Breath sauce, 15.2oz ringneck glass bottle. UPC on bottle: 7 01936 29222 3. There are 12 bottles per case. Manufactured Exclusively for BOOEYS GOURMET 3924 N. Cannon St. Spokane, WA

  Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame.

  Class II

• Medical Device Recall · March 23, 2026

  Olympus Corporation of the Americas

  Olympus Thunderbeat II Shears w/Ultrasonic Mode, 5mm, 35cm. Model Number: TB2-0535FC.

  Potential for detachment of a distal tip component of the device during use.

  Class II

• Food Recall · March 23, 2026

  BEF Foods, Inc

  Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g, product packed in plastic tub and placed into paperboard sleeve. 9/20 oz packages per case.

  Undeclared allergen (soy lecithin).

  Class II

• Drug Recall · March 21, 2026

  Buy-Herbal

  Kian Pee Wan Capsules, 30-count bottles

  Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.

  Class I

• Drug Recall · March 20, 2026

  Fagron Compounding Services

  Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5085-01

  Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

  Class II

• Medical Device Recall · March 20, 2026

  Centinel Spine, Inc.

  Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 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

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Honey Lemon Flavor, 30-count bag, Distributed By: CDMA Inc., Novi, MI 48375, Made in China, NDC: 83698-617-30, UPC: 635515986

  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

  Foundation Medicine, Inc.

  Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)

  Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants

  Class II

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Sugar Free, Black Cherry Flavor, 25-count bag, Distributed By: CDMA, Inc., Novi MI 48375, Made in China, NDC: 83698-616-25,

  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

• Vehicle Recall · March 20, 2026

  Grand Design RV, LLC

  2025 GRAND DESIGN LINEAGE

  Steps extending while in transit increase the risk of a crash.

  Unclassified

• Drug Recall · March 20, 2026

  Fagron Compounding Services

  norepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5026-02

  Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

  Class II

• Food Recall · March 20, 2026

  Bee Well Honey Farm & Supply Inc.

  Raw & Unfiltered Bee Well Wildflower Honey NET wT. 12 OZ (340g) UPC 8 32587 00003 2, NET WT. 22 OZ (624g) UPC 8 32587 00002 5 & NET WT. 44 OZ (1.25g) UPC 8 32587 00001 8 100% Pure Honey Bee Well Honey

  High sugar content. The firm was notified by the FDA that sample results were positive for a high C4 sugar content.

  Class III

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  Discount Drug Mart Food Market, Cough Drops, Menthol -Cough Suppressant Anesthetic, 30-count bag, Distributed By: Drug Mart-Food Fair, Medina, Ohio 44256, Made in China, NDC: 83698-102-30, UPC: 093351

  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

• Vehicle Recall · March 20, 2026

  Kia America, Inc.

  2027 KIA TELLURIDE HYBRID

  A person, especially a child, may become trapped by a rear powered seat, increasing the risk of injury.

  Unclassified

• Drug Recall · March 20, 2026

  Fagron Compounding Services

  Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5082-01

  Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

  Class II

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  MGC Health, Menthol- Cough Suppressant, Oral Anesthetic, Cough Drops, Honey Lemon, 80-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.

  MGC Health, Menthol- Cough Suppressant, Oral Anesthetic, Cough Drops, Sugar Free, Honey Lemon, 25-count bag, Distributed By: Medical Group Care, LLC, 1035 Collier Center Way, STE 5, Naples, FL 34110,

  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, Honey Lemon Flavor Cough Drops, 30-count bag, Manufactured for Your Military Exchanges By: Medical Group Care, LLC., 1035 Collier Center Wa

  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.

  QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, Distributed By: CDMA, Inc., Novi MI 48375, Made in China, NDC: 83698-616-25, UPC: 635515993372.

  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.

  QC Quality Choice, Pectin Oral Demulcent, Throat Soothing Drops, Creamy Strawberry Flavor, 30-count bag, Distributed By: CDMA, Inc., Novi, MI 48375, Made in China, NDC: 83698-625-30, UPC: 635515999398

  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

  Fagron Compounding Services

  norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02

  Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

  Class II

• Drug Recall · March 20, 2026

  Leading Pharma, LLC

  Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-118-01

  CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.

  Class II

• Drug Recall · March 20, 2026

  Xiamen Kang Zhongyuan Biotechnology Co., Ltd.

  QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Menthol Flavor, 30-count bag, Distributed By: CDMA Inc., Novi, MI 48375, Made in China, NDC: 83698-675-30, UPC: 635515986718.

  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.

  QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Vanilla Honey Flavor, 30-count bag, Distributed By: CDMA Inc., Novi, MI 48375, Made in China, NDC: 83698-620-30, UPC: 6355159

  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.

  caring mill, Menthol Cough Suppressant Oral Anesthetic, Cough Drops, Cherry, 90-count bag, Distributed by: FSA Store Inc., 5473 Blair Rd, Suite 100, PMB 24308, Dallas TX 75231, Made in China, NDC: 836

  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.

  QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Sugar Free, Honey Lemon Flavor, 25-count bag, Distributed By: CDMA, Inc., Novi, MI 48375, Made in China, NDC: 83698-616-25, U

  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

  Fagron Compounding Services

  Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01

  Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

  Class II