Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,114 results
Food & BeverageUSFDA Food

OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yusol International Foods Sacramento, CA 95828 Product of USA INGREDIENTS: Pounded Groundnuts (Intwilo) UPC: 650655764330

Fayus Inc.
FDA FoodClass II

OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yusol International Foods Sacramento, CA 95828 Product of USA INGREDIENTS: Pounded Groundnuts (Intwilo) UPC: 650655764330

Undeclared peanuts

Jul 22, 2026Fayus Inc.
Medical DeviceUSFDA Devices

Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F, 23F. heart pump and accessories.

Oscor Inc.
FDA DevicesClass I

Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F, 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, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device

Orthofix U.S. LLC
FDA DevicesClass II

Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, 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
Food & BeverageUSFDA Food

Ice Pop, D'Dioses Nanche, 1 Bar (81.7 g), with UPC 827912008449

D'Dioses Fruit Pops, Inc.
FDA FoodClass I

Ice Pop, D'Dioses Nanche, 1 Bar (81.7 g), with UPC 827912008449

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Jul 22, 2026D'Dioses Fruit Pops, Inc.
Food & BeverageUSFDA Food

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl. Cover. Cook for 1.5-2 minutes. Let sit 1 minute. Stir. Serve. Stovetop: Heat soup in a saucepan, stirring occasionally. AMY'S KITCHEN, INC. P.O. BOX 7129 PETALUMA, CA 94955 UPC (for U.S. product): 042272005833 UPC (for Canada product): 10042272905833

AMY'S KITCHEN INC.
FDA FoodClass II

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl. Cover. Cook for 1.5-2 minutes. Let sit 1 minute. Stir. Serve. Stovetop: Heat soup in a saucepan, stirring occasionally. AMY'S KITCHEN, INC. P.O. BOX 7129 PETALUMA, CA 94955 UPC (for U.S. product): 042272005833 UPC (for Canada product): 10042272905833

Potential for spoilage.

Jul 22, 2026AMY'S KITCHEN INC.
Food & BeverageFranceRappelConso

sans marque - jambon cuit sup avec son os ac

sans marque
RappelConsovolontaire (san...

sans marque - jambon cuit sup avec son os ac

présence de listeria

Jul 22, 2026sans marque
Medical DeviceUSFDA Devices

ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP; containing Introducer Product Code 0052-3006-JP. heart pump and accessories

Abiomed, Inc.
FDA DevicesClass I

ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP; 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

Arterial Line Kit 20ga x 6, REF: 400115A

Argon Medical Devices, Inc
FDA DevicesClass I

Arterial Line Kit 20ga x 6, REF: 400115A

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

Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Daavlin Distributing Company
FDA DevicesClass II

Photera 600, 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
Food & BeverageUSFDA Food

Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850

D'Dioses Fruit Pops, Inc.
FDA FoodClass I

Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Jul 22, 2026D'Dioses Fruit Pops, Inc.
Medical DeviceUSFDA Devices

ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204

Tosoh Bioscience Inc
FDA DevicesClass II

ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of testosterone in human serum on specific Tosoh AIA System analyzers, Model Number 0025204

The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could cause falsely elevated or falsely low total testosterone results. Such erroneous test results may lead to additional testing/diagnostic interventions and in limited cases, may lead to a delay in diagnosis and/or initiation of unnecessary or incorrect clinical treatment measures.

Jul 22, 2026Tosoh Bioscience 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

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
Medical DeviceUSFDA Devices

Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.

Olympus Corporation of the Americas
FDA DevicesClass II

Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.

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 Impella CP Set, Pump Set Code 0048-0014; containing Introducer Product Code 0052-3046. heart pump and accessories

Abiomed, Inc.
FDA DevicesClass I

ABIOMED Impella CP Set, Pump Set Code 0048-0014; 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

Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A

Argon Medical Devices, Inc
FDA DevicesClass I

Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A

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
Food & BeverageUSFDA Food

Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843

D'Dioses Fruit Pops, Inc.
FDA FoodClass I

Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843

May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.

Jul 22, 2026D'Dioses Fruit Pops, Inc.
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.
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
Medical DeviceUSFDA Devices

General Biospy Tray, REF: GUTS1000

Argon Medical Devices, Inc
FDA DevicesClass I

General Biospy Tray, REF: GUTS1000

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

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
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
Medical DeviceUSFDA Devices

ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump

ICU Medical, Inc.
FDA DevicesClass II

ICU Medical Plum Solo Precision IV Pump, v1.0.3, Item Number 400010401; infusion pump

In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate.

Jul 22, 2026ICU Medical, 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

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