Safety Recalls

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

Showing 3,001–3,050 of 17,559

• Consumer Product Recall · March 19, 2026

  Shenzhenshiyongxintaidianziyouxiangongsi (Shenzhen Yongxintai Electronics Co., Ltd.), dba, Yxtdz Store, of China

  Aisstxoer Adult Bike Helmets

  The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

  Unclassified

• Medical Device Recall · March 19, 2026

  Boston Scientific Corporation

  Boston Scientific Cardiac Resynchronization Therapy (CRT)labeled as: 1. VALITUDE CRT-P EL, Model Number U125; 2. VALITUDE CRT-P EL MRI, Model Number U128; 3. VISIONIST CRT-P EL, Model Number U2

  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: SPNG NEURO 1X1 10/PK XR, Medline Kit Number/SKU DNSC38133

  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

• Drug Recall · March 19, 2026

  Teva Pharmaceuticals USA, Inc

  Clonidine Transdermal System, USP, 0.3 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake City, UT 84108, Distributed by:

  CGMP Deviations: use of an unapproved raw material

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges (102 in total)

  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 (4077 in total), LAMINECTOMY, CRANI, 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

  Centurion medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SURGICAL ENT PREP KIT, Medline Kit Number/SKU MNS11715

  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: PEDS AIRWAY PACK, Medline Kit Number SKU DYNJ86657A

  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/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product Description: 11-1424 - ICEMAN W/,UNIV,LOOP,NS,EH The IceMan CLASSIC3¿ cold th

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

  Class II

• Consumer Product Recall · March 19, 2026

  Amazon.com Services LLC, of Seattle, Washington

  Amazon Basics Camping Folding Pocket Knives

  The folding mechanism on the blade can fail to remain properly secured in the closed position, posing a laceration hazard.

  Unclassified

• Consumer Product Recall · March 19, 2026

  Lifetime Brands, Inc., owner of the BUILT brand, of Garden City, New York

  BUILT LUUM Tumblers

  The recalled LED tumblers can break, making the button cell batteries accessible to children and posing choking and ingestion hazards. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. SPINE PROCEDURES PACK-LF, Medline Kit Number/SKU DYNJ0751220P; 2. ENSEMBLE RACHIS-LF, 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

• Drug Recall · March 19, 2026

  Teva Pharmaceuticals USA, Inc

  Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake City, UT 84108, Distributed by:

  CGMP Deviations: use of an unapproved raw material

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. NEURO BASIN PACK-LF, Medline Kit Number/SKU DYNJ0532910L; 2. NEURO BASIN PACK-LF, Medline Kit Number/SKU D

  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 Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.25" X 0.25", XR, 10/PK, Medline SKU NEUROSPNG02; 2. Neuro Sponges, Eponges 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

• Food Recall · March 19, 2026

  Riverence Provisions LLC

  Riverence Smoked Trout Dip, net wt. 7oz. Product is perishable, refrigerated, packaged in plastic tub. Product is shipped to consignee frozen by the case (12/7oz. units per case). Retail container U

  Label declares cream cheese but does not declare milk

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. OSC COLEMAN FAT HARVEST KIT, Medline Kit Number/SKU DYNJ32854B; 2. RR-DR. CHHETRI MDL PACK, Medline Kit Nu

  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

  Electrolux Consumer Products, Inc., of Charlotte, North Carolina

  Frigidaire Gas Ranges

  The ovens in the ranges can experience a delayed ignition of the oven's bake burner, posing a risk of burn hazards to users.

  Unclassified

• Drug Recall · March 19, 2026

  Teva Pharmaceuticals USA, Inc

  Clonidine Transdermal System, USP, 0.1 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx Only, Manufactured by: Actavis Laboratories UT Inc., Salt Lake City, UT 84108, Distributed by:

  CGMP Deviations: use of an unapproved raw material

  Class II

• Medical Device Recall · March 19, 2026

  Medline Industries, LP

  Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. ENDOSCOPIC SKULL BASE, Medline Kit Number/SKU DYNJ58648J; 2. ENT ENDO SINUS WILMINGTON PACK, Medline Kit Nu

  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: CERVICAL PACK, Medline Kit Number/SKU DYNJ37902F

  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

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device (Interventional Tool) intended to be used in combination with a Philips interventional X-ray system and 3DRA d

  Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA ratio does not provide reliable prognostic information regarding aneurysm occlusion following Flow Diverter Stent treatment, however despite being stated in the IUF, it is being relied on for making clinical decisions.

  Class II

• Medical Device Recall · March 18, 2026

  Diversatek Healthcare

  Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator, 6mm-7mm-8mm, REF 1204-08

  The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.

  Class II

• Medical Device Recall · March 18, 2026

  Diversatek Healthcare

  Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 12mm-13.5mm-15mm, REF 1205-15

  The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.

  Class II

• Drug Recall · March 18, 2026

  Island Kinetics, Inc. d.b.a. CoValence Laboratories

  Remedy Gel, hydrocortisone 1%, 30 mL/ 1 fl oz per bottle, Distributed By: glo Skin Beauty, Denver, CO 80216. NDC 66915-531-12; 66915-531-13

  Subpotent Drug

  Class III

• Medical Device Recall · March 18, 2026

  Diversatek Healthcare

  Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 15mm-16.5mm-18mm, REF 1205-18

  The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.

  Class II

• Medical Device Recall · March 18, 2026

  Diversatek Healthcare

  Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 18mm-19mm-20mm, REF 1205-20

  The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.

  Class II

• Medical Device Recall · March 18, 2026

  Siemens Healthcare Diagnostics, Inc.

  Dimension Creatinine Flex reagent cartridge. Material Number: 10872079.

  Siemens Healthcare Diagnostics is recalling certain lots of Dimension Creatinine Flex reagent cartridge (Dimension CRE2) because a potential imprecision in the Dimension CRE2 quality control (QC) and patient sample results using lot numbers GA6307 and BA7005 on the Dimension System. This imprecision may lead to erroneously decreased or increased creatinine patient results

  Class II

• Vehicle Recall · March 18, 2026

  Keystone RV Company

  2026 KEYSTONE MONTANA

  Damaged wiring may cause an electrical fault, increasing the risk of a fire.

  Unclassified

• Drug Recall · March 18, 2026

  Island Kinetics, Inc. d.b.a. CoValence Laboratories

  Essential Calming Skin Gel, hydrocortisone 1%, 120mL/4oz net wt. (113g) per jar, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM, NDC 66915-531-05

  Subpotent Drug

  Class III

• Drug Recall · March 18, 2026

  Island Kinetics, Inc. d.b.a. CoValence Laboratories

  Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone 1%, .53oz net wt. (15.3g) per bottle, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM. NDC 66915-5

  Subpotent Drug

  Class III

• Drug Recall · March 18, 2026

  Amneal Pharmaceuticals, LLC

  Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV bags, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad, 382110,

  Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.

  Class I

• Vehicle Recall · March 17, 2026

  Ford Motor Company

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

  A loose seat belt buckle may not properly restrain an occupant during a crash, increasing the risk of injury.

  Unclassified

• Drug Recall · March 17, 2026

  Nephron SC, LLC

  Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only, nephron 503B Outsourcing facility, 4600 12th Street Extension, West Columbia, SC 29172, ND

  Labelling: Illegible label

  Class II

• Drug Recall · March 17, 2026

  Teva Pharmaceuticals USA, Inc

  Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greec

  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 · March 17, 2026

  Straumann USA LLC

  Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;

  A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.

  Class II

• Drug Recall · March 17, 2026

  Teva Pharmaceuticals USA, Inc

  Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 20 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greec

  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 · March 17, 2026

  Medical Action Industries, Inc. 306

  Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

  Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

  Class I

• Medical Device Recall · March 17, 2026

  Straumann USA LLC

  Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;

  A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.

  Class II

• Drug Recall · March 17, 2026

  Teva Pharmaceuticals USA, Inc

  Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 10 mg, Single-dose 8 mL vial in Kit, Rx only, Manufactured in Greece BY: Pharmathen International S.A, Rodopi, 693 00 Greec

  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

• Vehicle Recall · March 17, 2026

  Ford Motor Company

  2025 FORD F-53, 2026 FORD F-59

  Brake lights that remain illuminated can fail to alert other vehicles of the driver's intention, increasing the risk of a crash.

  Unclassified

• Drug Recall · March 17, 2026

  Viatris, Inc.

  Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC, Morgantown, WV 06506, U.S.A, Made in Ireland, NDC 58151-506-91

  Failed Dissolution Specifications

  Class II

• Drug Recall · March 17, 2026

  Chiesi USA, Inc.

  CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03.

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · March 16, 2026

  Medline Industries, LP

  Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: LATEX FREE GENERAL PURPOSE TRAY, Medline Kit SKU 75670

  Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

  Class II

• Medical Device Recall · March 16, 2026

  Beckman Coulter, Inc.

  Access Total T4 Calibrator, Catalog No. 33805

  Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product specifications. A false low patient result could cause a patient to undergo unnecessary additional diagnostic testing. A patient may be treated for a disorder not present or receive delayed treatment for hyperthyroidism. For a pregnant patient being monitored for thyroid hormone supplementation, incorrect treatment or dose may be used. A delayed patient results could cause repeat blood draw with associated complications.

  Class II

• Medical Device Recall · March 16, 2026

  Medline Industries, LP

  Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: DERMATOLOGY SHAVE KIT, Medline Kit SKU SK395

  Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

  Class II

• Medical Device Recall · March 16, 2026

  SurgiSmoke Solutions

  Flamingo Funnel Medium, Model Number SQ20012-02

  Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.

  Class II

• Medical Device Recall · March 16, 2026

  Smith & Nephew, Inc.

  TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816

  Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before implantation, an equivalent backup can be used, or a bent nail of the same size, which would require additional surgical steps to address soft tissue/bone preparation, which could lead to a surgical delay of greater than 30 minutes.

  Class II

• Food Recall · March 16, 2026

  Albertsons Companies LLC

  Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt.24oz. Perishable and keep refrigerated. Consumer package is a plastic cup with foil lid and clear plastic lid. UPC 0 211

  Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in coil width. Spring ends are not sharp but may be sharp if broken/ cut.

  Class II

• Drug Recall · March 16, 2026

  Cipla USA, Inc.

  Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300,

  CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit

  Class II