Safety Recalls

17,395 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,451–1,500 of 17,395

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI Code: 0110885403108365 TPT1000 THORACENTESIS/PARACENTESIS TRAY UDI-DI Co

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Windstone Medical Packaging, Inc.

  A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit

  Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

  Class I

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108501 The Soft Tissue Biopsy devices are indicated for use in the col

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) ARTERIAL LINE KIT, Model Number: ART890B; 2) ULTRASOUND GUIDED IV SECUREMENT SET, Model Number: IVS3350

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Laborie Medical Technologies Corp

  Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar GI HRM H2O, 24p, Compact Pole system (G3-7), Solar GI HRM H2O, 24p, Trolley syst

  Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed.

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 PowerPICC SOLO Catheter 5 Fr Dual-Lumen UDI-DI Code: 00801741034602 1174108D3 PowerPICC Catheter 4 Fr Single-Lu

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Drug Recall · May 21, 2026

  Keystone Industries

  Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Contents: 1 oz (3o g), Manufactured for: Pearson Dental Supply Inc., Sylmar, CA 91342 USA, NDC 43305-0009-3.

  Defective container:may contain bottles with incomplete seals

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Provena Midline Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154003 S4153108BP Provena Midline Cath

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Baxter Healthcare Corporation

  Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung Expansion Therapy, positive pressure breathing device

  There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

  Class I

• Drug Recall · May 21, 2026

  Keystone Industries

  PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life, LLC, Manufactured for PureLife LLC., Carson, CA 90810. NDC 68987-001-30

  Defective container:may contain bottles with incomplete seals

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM, Model Number: ECVC8520; 2) NO CATH CENTRAL LINE KIT, Model Number: CVI4880B; 3) 20G x 6" ARTERIAL CATHETER KIT, Model Number: ART356; 4) MULTI

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Karl Storz Endoscopy

  Flexible Hystero-Fiberscope Kits REF: 11264BBU1, 11264BBUK1, that contain expired Single Use Endoscopic Seal: GYN, REF: 26153EAU/1.

  Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use, which could impact the assurance of sterility.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Pro Wireguided 18-20mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Pro Wireguided 8-10mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Vehicle Recall · May 21, 2026

  Nissan North America, Inc.

  2025 NISSAN KICKS

  A partial or blank screen display will not show critical safety information such as vehicle speed and warning lights, increasing the risk of a crash.

  Unclassified

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) DYNJ0621189X, Model Number: SM RADIOLOGY-ANGIO PACK-LF; 2) PAIN1470A, Model Number: CONT. 20G EPI MRI COMPATIBLE; 3) TVS4000L, Model Number: TVS4000 ENDOVENOUS PACK

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Baxter Healthcare Corporation

  Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung Expansion Therapy, positive pressure breathing device

  There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

  Class I

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO, Model Number: DYNJ57922A

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Pro Wireguided 10-12mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Drug Recall · May 21, 2026

  Keystone Industries

  Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30 g), Distributed by Dental City, 3205 Yeager Dr., Green Bay, WI 54311. NDC 69483-001-30

  Defective container:may contain bottles with incomplete seals

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY, Model Number: CIT6780; 2) CIRCUMCISION TRAY W/1.1CM CIRCLAMP, Model Number: CIT3225A; 3) CIRCUMCISION TRAY, Model Number: CIT6325

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) IMAGING BIOPSY TRAY, Model Number: DYNDH1068; 2) BREAST BIOPSY PACK, Model Number: PHS234706I

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI Code: 00801741107177 5855300 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Pro Wireguided 15-18mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC SV Catheter 3 Fr Single-Lumen REKV2227 00801741027536 The PowerPlCC SV catheters are intended for shor

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Papablic Inc

  Papablic Replacement Brush Heads. Model Number: PAPA317AA.

  Potential for brush heads to break.

  Class II

• Consumer Product Recall · May 21, 2026

  ABC Trading Inc., of Vernon, California

  WSDZ Light-up Shot Glasses

  The recalled glasses violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries can be accessed easily by children, posing an ingestion hazard. Additionally, the packaging and product do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · May 21, 2026

  Supa Products Pte Ltd., dba HomeProGym, of Singapore

  HomeProGym Resistance Bands

  The recalled resistance bands can forcefully separate from the handle during use, posing a risk of serious injury from impact hazard.

  Unclassified

• Medical Device Recall · May 21, 2026

  Baxter Healthcare Corporation

  Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M08474; Oscillation Lung Expansion Therapy, positive pressure breathing device

  There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

  Class I

• Food Recall · May 21, 2026

  Galliker Dairy Co, Inc.

  DQ Chocolate Reduced Fat Ice Cream Mix, 5 GAL (18.9L). Keep refrigerated.

  Foreign material found in product (identified as metal shavings)

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 CK000566 Poly Midline Catheter 4 Fr S

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Elekta, Inc.

  MOSAIQ Oncology Information System

  Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Wireguided 12-15mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Wireguided 15-18mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Medical Device Recall · May 21, 2026

  Baxter Healthcare Corporation

  Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270; Oscillation Lung Expansion Therapy, positive pressure breathing device

  There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

  Class I

• Consumer Product Recall · May 21, 2026

  ABC Trading Inc., of Vernon, California

  Toy Headbands, Electronic Pet Cage-Dinosaur Tribes, My Pet Bird Cute Bird Tribes

  The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · May 21, 2026

  Bethlehem Lights LLC, of Naperville, Illinois

  Bethlehem Lights 10-inch Illuminated Ribbon Spheres

  The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.

  Unclassified

• Consumer Product Recall · May 21, 2026

  Lil Pick Up Inc., of Rowland Heights, California

  Sierra 125U Youth All-Terrain Vehicles (ATVs)

  The recalled youth ATVs violate the federal mandatory ATV safety standard, posing a risk of serious injury or death. The youth ATVs fail to meet mechanical suspension requirements, and the reverse indicator light fails to illuminate, posing a crash hazard. The parking brakes fail to hold, posing a collision hazard. Additionally, the surfaces near the footwell can reach high temperatures, posing a risk of severe burns.

  Unclassified

• Consumer Product Recall · May 21, 2026

  The Orb Factory Limited, dba ORB Toys, of Canada

  Orb Funkee Squeeze Toys

  The recalled Orb Funkee squeeze toys may contain fibrous tremolite (asbestos) in the sand, which can cause adverse health issues if inhaled.

  Unclassified

• Consumer Product Recall · May 21, 2026

  PandaEar of Lake Dallas, Texas and Rockville, Maryland

  Portable Hook-On Chairs

  The recalled portable hook-on chairs violate the mandatory standard for portable hook-on chairs because the crotch restraints can be removed without the use of a tool and infants can fall through an opening, posing a deadly fall hazard.

  Unclassified

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  BD SWITZERLAND SARL

  BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or exte

  Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable.

  Class II

• Medical Device Recall · May 21, 2026

  Windstone Medical Packaging, Inc.

  A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit

  Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

  Class I

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) STD, INTRO-FLEX INTRODUCER 6F, C, Model Number: I550BF6C; 2) STD, INTRO-FLEX INTRODUCER 9F, C, Model Number: I505BF9C

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Bard Access Systems, Inc.

  CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylets provide internal reinforcement to aid in catheter placement.

  Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

  Class II

• Medical Device Recall · May 21, 2026

  Instrumentation Laboratory

  GEM Premier 7000 with iQM3 Part Numbers: 00077407508 00077407510 00077415004 00077415008 00077415010 00077430010 Product Description: The GEM Premier 7000 with iQM3 is a portable critic

  The active ingredient concentration in the lysing bag solution of specific GEM Premier 7000 with iQM3 PAK lots did not meet established manufacturing specifications. The malfunction could result in delayed recognition and management of Co-Oximetry and total bilirubin abnormalities and their sequelae.

  Class II

• Medical Device Recall · May 21, 2026

  Medline Industries, LP

  Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE, Model Number: ART1145; 2) Universal Central/Art Line Insertion Kit, Model Number: ART155A; 3) ARTERIAL LINE INSERTION TRAY, Model Nu

  The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Wireguided 6-8mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II

• Medical Device Recall · May 21, 2026

  Medical Action Industries, Inc. 306

  Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791

  Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.

  Class II

• Medical Device Recall · May 21, 2026

  Boston Scientific Corporation

  CRE Wireguided 8-10mm 240cm

  Potential sterile breach of the pouches in which devices are packaged.

  Class II