Estados Unidos Recalls

Retiros de seguridad del consumidor de la FDA, CPSC, NHTSA y USDA FSIS.

Showing 24 of 17,562 results
Medical DeviceUSFDA Devices

da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15

Intuitive Surgical, Inc.
FDA DevicesClass II

da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15

Robotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the product, which may expose a section of instrument arm, which may result in procedure delay or conversion to an alternate minimally invasive approach. Retrospectively reported recall.

Jul 22, 2026Intuitive Surgical, Inc.
Medical DeviceUSFDA Devices

Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The device delivers airflow from a PAP device to the patient's nose and is secured using adjustable headgear. Component: No

3B Medical, Inc.
FDA DevicesClass II

Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The device delivers airflow from a PAP device to the patient's nose and is secured using adjustable headgear. Component: No

Packaging and labeling discrepancy involving product size identification and associated Unique Device Identifier (UDI/GTIN).

Jul 22, 20263B Medical, Inc.
Medical DeviceUSFDA Devices

ABIOMED Impella CP Set, Pump Set Code 0048-0044; containing Introducer Product Code 0052-3046. heart pump and accessories

Abiomed, Inc.
FDA DevicesClass I

ABIOMED Impella CP Set, Pump Set Code 0048-0044; containing Introducer Product Code 0052-3046. heart pump and accessories

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

Jul 22, 2026Abiomed, Inc.
Medical DeviceUSFDA Devices

Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A.

Olympus Corporation of the Americas
FDA DevicesClass II

Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A.

Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.

Jul 22, 2026Olympus Corporation of the Americas
Medical DeviceUSFDA Devices

Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F 13cm and 25cm. heart pump and accessories.

Oscor Inc.
FDA DevicesClass I

Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F 13cm and 25cm. heart pump and accessories.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region.

Jul 22, 2026Oscor Inc.
Food & BeverageUSFDA Food

Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC 107-21582-13283-1. Keep Frozen. Case Qty 180. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.

General Mills James Ford Bell Technical Center
FDA FoodClass II

Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC 107-21582-13283-1. Keep Frozen. Case Qty 180. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.

Potential foreign material (glass)

Jul 22, 2026General Mills James Ford Bell Technical Center
Medical DeviceUSFDA Devices

Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J

Medline Industries, LP
FDA DevicesClass II

Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J

Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of product include clinically insignificant extension of surgery to find another readily available device.

Jul 22, 2026Medline Industries, LP
PharmaceuticalUSFDA Drugs

Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.

Bell Pharmaceuticals, Inc
FDA DrugsClass II

Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
Medical DeviceUSFDA Devices

Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Daavlin Distributing Company
FDA DevicesClass II

Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000).

Jul 22, 2026Daavlin Distributing Company
Medical DeviceUSFDA Devices

Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 23F. heart pump and accessories.

Oscor Inc.
FDA DevicesClass I

Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 23F. heart pump and accessories.

Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region.

Jul 22, 2026Oscor Inc.
Medical DeviceUSFDA Devices

Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external fixation device

Orthofix U.S. LLC
FDA DevicesClass II

Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external fixation device

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

Jul 22, 2026Orthofix U.S. LLC
PharmaceuticalUSFDA Drugs

GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit - Washer Bulb Included, (NDC 46122-556-05); b) 1 bottle (NDC 46122-557-05), Distributed by: AmerisourceBergen, 1 West First Avenue, Conshohocken, PA 19428.

Bell Pharmaceuticals, Inc
FDA DrugsClass II

GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit - Washer Bulb Included, (NDC 46122-556-05); b) 1 bottle (NDC 46122-557-05), Distributed by: AmerisourceBergen, 1 West First Avenue, Conshohocken, PA 19428.

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
PharmaceuticalUSFDA Drugs

AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb Included (NDC 59256-001-02); b) 1 bottle (NDC 59256-836-34), Distributed By: Oaktree Products Inc., St. Louis. MO 63005.

Bell Pharmaceuticals, Inc
FDA DrugsClass II

AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb Included (NDC 59256-001-02); b) 1 bottle (NDC 59256-836-34), Distributed By: Oaktree Products Inc., St. Louis. MO 63005.

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
PharmaceuticalUSFDA Drugs

CVS Health, Carbamide Peroxide, 6.5%, 0.5 FL Oz (15 mL), a) Bottle (NDC 51316-822-00.); b) Kit (1 BULB, Syringe & Drops- NDC 51316-823-00.), Distributed by: CVS Pharmacy., Inc. One CVS Drive, Woonsocket, RI 02895,

Bell Pharmaceuticals, Inc
FDA DrugsClass II

CVS Health, Carbamide Peroxide, 6.5%, 0.5 FL Oz (15 mL), a) Bottle (NDC 51316-822-00.); b) Kit (1 BULB, Syringe & Drops- NDC 51316-823-00.), Distributed by: CVS Pharmacy., Inc. One CVS Drive, Woonsocket, RI 02895,

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
PharmaceuticalUSFDA Drugs

TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS INCLUDED (NDC 36800-835-33); b) 1 bottle (NDC 36800-835-34), DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007.

Bell Pharmaceuticals, Inc
FDA DrugsClass II

TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS INCLUDED (NDC 36800-835-33); b) 1 bottle (NDC 36800-835-34), DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007.

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
Medical DeviceUSFDA Devices

ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460; containing Introducer Product Code 0052-3006-JP. heart pump and accessories

Abiomed, Inc.
FDA DevicesClass I

ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460; containing Introducer Product Code 0052-3006-JP. heart pump and accessories

A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.

Jul 22, 2026Abiomed, Inc.
Medical DeviceUSFDA Devices

T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL

Argon Medical Devices, Inc
FDA DevicesClass I

T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Jul 22, 2026Argon Medical Devices, Inc
Medical DeviceUSFDA Devices

The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.

Maquet Cardiovascular, LLC
FDA DevicesClass II

The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.

Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-28782A) performed by STERIS at its Whippany, NJ facility between March 31 and April 1 of 2026.

Jul 22, 2026Maquet Cardiovascular, LLC
Medical DeviceUSFDA Devices

Optima XR240amx, Mobile Digital Radiographic System

GE Medical Systems, LLC
FDA DevicesClass II

Optima XR240amx, Mobile Digital Radiographic System

GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been performed to confirm proper assembly. If a failure of the internal counterpoise cable occurs, the Column Safety mechanism will not work, causing the arm with X-ray tube and collimator to drop downward on the column track. This could result in patient injury during an exam.

Jul 22, 2026GE Medical Systems, LLC
Medical DeviceUSFDA Devices

Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula

Medtronic Perfusion Systems
FDA DevicesClass II

Medtronic Bio-Medicus Adult Cannula Kit, Product Number/CFN 96530-115; Cardiopulmonary bypass vascular cannula

Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.

Jul 22, 2026Medtronic Perfusion Systems
PharmaceuticalUSFDA Drugs

Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx only, 15 g tube, Manufactured by Padagis, Yeruham, Israel, NDC 45802-059-35

Padagis US LLC
FDA DrugsClass II

Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx only, 15 g tube, Manufactured by Padagis, Yeruham, Israel, NDC 45802-059-35

Subpotent Drug: Low out of specification assay results performed during long-term stability testing.

Jul 22, 2026Padagis US LLC
PharmaceuticalUSFDA Drugs

meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.

Bell Pharmaceuticals, Inc
FDA DrugsClass II

meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
Medical DeviceUSFDA Devices

One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular

Argon Medical Devices, Inc
FDA DevicesClass I

One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular

Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.

Jul 22, 2026Argon Medical Devices, Inc
Medical DeviceUSFDA Devices

Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF: M122, Unilateral orthopedic/trauma external fixation device

Orthofix U.S. LLC
FDA DevicesClass II

Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF: M122, Unilateral orthopedic/trauma external fixation device

Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111

Jul 22, 2026Orthofix U.S. LLC

Install The Recall File App

Check safety warnings, scan your pantry, and monitor your vehicles directly from your home screen.