DrugJan 24, 2024
The Procter & Gamble Company Old Spice, PURE SPORT recall — FDA D-0238-2024
Chemical contamination: presence of benzene
Class IFDA: TerminatedThe Procter & Gamble Company
January 2024 recalls — page 7
These records include useful source details for the selected month.
DrugJan 24, 2024
Ibuprofen and Famotidine Tablets 800mg/26.6mg recall — FDA D-0237-2024
Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
Class IIFDA: OngoingAscend Laboratories, LLC
DrugJan 24, 2024
Vasostrict recall — FDA D-0232-2024
Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.
Class IIFDA: OngoingPar Sterile Products LLC
DrugJan 24, 2024
The Procter & Gamble Company Secret, Dry Spray, Aluminum chlorohydrate 23.5% recall — FDA D-0244-2024
Chemical contamination: presence of benzene
Class IFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
SECRET ANTIPERSPIRANT Secret, powder fresh recall — FDA D-0253-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Old Spice, SWEAT DEFENSE PURE SPORT PLUS recall — FDA D-0251-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum recall — FDA D-0252-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Secret, OUTLAST, Dry Spray recall — FDA D-0247-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
SECRET ANTIPERSPIRANT Secret, powder fresh, Aluminum chlorohydrate 24% recall — FDA D-0242-2024
Chemical contamination: presence of benzene
Class IFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Old Spice Pure Sport 2021 Gift Set, Contains: Old Spice Pure recall — FDA D-0249-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
Pfizer 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit recall — FDA D-0233-2024
Presence of Particulate Matter; identified as glass
Class IFDA: OngoingPfizer Inc.
DrugJan 24, 2024
The Procter & Gamble Company Secret OUTLAST Dry Spray recall — FDA D-0248-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
MAGNESIUM CITRATE Good Neighbor Pharmacy, DYE FREE, SUGAR FREE Magnesium Citrate Saline recall — FDA D-0227-2024
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Class IIFDA: OngoingPharma Nobis LLC
VehicleJan 22, 2024
Tesla camera recall — NHTSA campaign 24V035000
Tesla, Inc. (Tesla) is recalling certain 2023 Model S, X, and Y vehicles equipped with full self-driving computer 4.0 and running a software release version 2023.44.30 through 2023.44.30.6…
cameraTesla, Inc.
VehicleJan 19, 2024
Explorer roof and pillars recall — NHTSA campaign 24V031000
Ford Motor Company (Ford) is recalling certain 2011-2019 Explorer vehicles. The A-pillar trim retention clips may not be properly engaged, allowing the trim to detach.
roof and pillarsFord Motor Company
VehicleJan 18, 2024
Kia roof and pillars recall — NHTSA campaign 24V025000
Kia America, Inc. (Kia) is recalling certain 2023-2024 Sportage and 2022-2024 Carnival vehicles. The roof molding may loosen and detach.
roof and pillarsKia America, Inc.
Medical DeviceJan 17, 2024
Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x recall — FDA Z-0643-2024
The internal diameter of the coaxial cannula may be smaller or larger than the external diameter of the biopsy needle, and the length of the cannula may exceed the stated length on the…
Class IIFDA: OngoingBard Peripheral Vascular Inc.
Medical DeviceJan 17, 2024
Baxter Healthcare Peri-Guard Repair Patch, Product Codes: a) PC1016NBIO: 10X16CMUS, b) recall — FDA Z-0665-2024
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJan 17, 2024
Baxter Healthcare XScribe Cardiac Stress Testing System, version 6, with below product names recall — FDA Z-0706-2024
Potential distortion identified in electrocardiogram (ECG) readings when the Source Consistency Filter (SCF) is enabled.
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJan 17, 2024
Baxter Healthcare Q-Stress Cardiac Stress Testing System, version 6, with below product name recall — FDA Z-0705-2024
Potential distortion identified in electrocardiogram (ECG) readings when the Source Consistency Filter (SCF) is enabled.
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJan 17, 2024
Baxter FloSeal Hemostatic Matrix RECOTHROM, Product Codes: a) ADS202105, 5mL-6 PK US b) recall — FDA Z-0662-2024
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJan 17, 2024
Abiomed KIT, 14 Fr Introducer, 13 & 25 cm, ABMD Part of Pump Set recall — FDA Z-0654-2024
Hole(s) to the outer pouch of the Introducer Kits (both trayed and non-trayed) may compromise the sterile barrier of the Introducer Kits. Non-sterile product exposes patients to the…
Class IIFDA: OngoingAbiomed, Inc.
Medical DeviceJan 17, 2024
Baxter Healthcare Peri-Guard Repair Patch, Product Codes: a) PG1016 : 10 X 16 CMUS, TS b) recall — FDA Z-0664-2024
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJan 17, 2024
Baxter Vascular Probe, Product Codes: a) 7081015: 8CM, 1- 1.5 MM GLOBAL, b) 7081520: 8CM recall — FDA Z-0659-2024
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products…
Class IIFDA: OngoingBaxter Healthcare Corporation
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.