Recalls in January 2026 (page 2)
471 recalls.
- Claviculaplate with Angular Stability recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Volar Radius Plate with Angular Stability with the following description: Radius Plate... recall (I.T.S. GmbH)
Medical deviceClass IIReported April 1, 2026 · Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for... - Simply Nature recall (Dr. Praeger's Sensible Foods Inc.)
FoodClass IIReported March 25, 2026 · This product has the possibility of contamination with rodent hair. - Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported March 25, 2026 · There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local... - Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported March 25, 2026 · There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local... - Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported March 25, 2026 · There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local... - VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz recall (Palmetto Gourmet Foods Inc.)
FoodClass IIReported March 18, 2026 · Product contains undeclared Yellow #5 - VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz recall (Palmetto Gourmet Foods Inc.)
FoodClass IIReported March 18, 2026 · Product contains undeclared Yellow #5 - Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE recall (Medline Industries, LP)
Medical deviceClass IIReported March 18, 2026 · Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may... - Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN recall (Medline Industries, LP)
Medical deviceClass IIReported March 18, 2026 · Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may... - Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported March 18, 2026 · The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target... - CLARITY II Laser System recall (Lutronic Corporation)
Medical deviceClass IIReported March 18, 2026 · Reports of devices sparking/popping and potentially burning patients. - HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product... recall (Covidien LLC)
Medical deviceClass IIReported March 18, 2026 · Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on the remote... - CHEMISTRY ANALYZER AU5800 recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported March 18, 2026 · A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15... - DxC 700 AU recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported March 18, 2026 · A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15... - Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm recall (Medartis AG)
Medical deviceClass IIReported March 18, 2026 · Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws. - Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm recall (Medartis AG)
Medical deviceClass IIReported March 18, 2026 · Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws. - PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers:... recall (Physio-Control, Inc.)
Medical deviceClass IIReported March 18, 2026 · Due to pediatric defibrillator electrode delamination - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - GEM Premier 5000 PAK recall (Instrumentation Laboratory)
Medical deviceClass IIReported March 18, 2026 · Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution... - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model SL Connection Component incl. PE-Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model SL Connection Component incl. PE-Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model Replacement Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Endo-Model SL Connection Component incl. PE-Plateau recall (Waldemar Link GmbH & Co. KG (Mfg Site))
Medical deviceClass IIReported March 18, 2026 · The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture. - Raz-AT recall (Raz Design Inc)
Medical deviceClass IIReported March 18, 2026 · Due to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in place. - 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk... recall (Becton Dickinson & Company)
Medical deviceClass IIReported March 18, 2026 · During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes. - MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE recall (KOB GmbH)
Medical deviceClass IIReported March 18, 2026 · Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine. - Karns Foods recall (Karns Prime And Fancy Foods)
FoodClass IReported March 11, 2026 · Product may contain undeclared peanuts. - Premium Food Bubble Gum recall (Bader Enterprises, Inc.)
FoodClass IIReported March 11, 2026 · Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake). - Premium Food Jordan Almonds recall (Bader Enterprises, Inc.)
FoodClass IIReported March 11, 2026 · Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake). - Sodium Iodide recall (Radnostix)
DrugClass IIReported March 11, 2026 · Presence of Particulate Matter: Due to production issues - Antimicrobial Alcohol Hand Wipe recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Children's Healthcare of Atlanta recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dynarex recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dynarex recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Green Guard Antiseptic Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Hand Sanitizing Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - WP WipesPlus Hand Sanitizing Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Med-Nap Cleansing Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Cleansing Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dynarex Obstetrical Towelettes Cleanser recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Wipes Plus recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Med Nap BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Medi-First Antiseptic Wipes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Savannah Antibacterial Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Max Packaging Antibacterial Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - 1) BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Dukal BZK Antiseptic Towelette recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - First Aid Only BZK Antiseptic Towelettes recall (ACME UNITED CORPORATION)
DrugClass IIReported March 11, 2026 · CGMP Deviations - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Metoprolol Succinate Extended-Release Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name:... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Mis-wired component-the improperly wired component can result in additional noise on the power supply output. Noise on the ultrasonic input circuit is not... - Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. ... recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported March 11, 2026 · Potential for rubber fragment detachment during use. - CS300 IABP. Software Version CS300 IABP C.01. recall (Datascope Corp.)
Medical deviceClass IIReported March 11, 2026 · The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated. - CS100 IABP. Software Version CS100 IABP Q.01. recall (Datascope Corp.)
Medical deviceClass IIReported March 11, 2026 · The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated. - Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM ... recall (Aesculap Inc)
Medical deviceClass IIReported March 11, 2026 · There is the potential for the length of the trocar shaft to be too long. - Atellica CH Urine Albumin recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported March 11, 2026 · Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL may... - EVO+ Visian Toric Implantable Collamer Lens recall (Staar Surgical AG)
Medical deviceClass IIReported March 11, 2026 · Toric Implantable Collamer for correction/reduction of myopia in phakic eyes with astigmatism were labeled as 12.1 mm length but are 12.6 mm length lenses, so... - cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported March 11, 2026 · Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is an... - GE Healthcare Centricity Universal Viewer Zero Footprint Client recall (GE Healthcare)
Medical deviceClass IIReported March 11, 2026 · Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP)... - Impella RP. Product Code: 0046-0011. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Impella RP Flex with SmartAssist. Product Code: 1000323. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - Impella RP with SmartAssist. Product Code: 0046-0035. recall (Abiomed, Inc.)
Medical deviceClass IReported March 11, 2026 · Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift. - NAVITAS ORGANICS ORGANIC CHIA SEEDS recall (Navitas, LLC.)
FoodClass IReported March 4, 2026 · Potential contamination with Salmonella. - Fish Ball recall (MIN JIANG FOOD STORE INC DBA KOI KOI TRADING)
FoodClass IReported March 4, 2026 · Undeclared allergen ingredient (Wheat and Sesame) - Fish Ball recall (MIN JIANG FOOD STORE INC DBA KOI KOI TRADING)
FoodClass IReported March 4, 2026 · Undeclared allergen ingredient (Wheat and Sesame) - Fish Ball recall (MIN JIANG FOOD STORE INC DBA KOI KOI TRADING)
FoodClass IReported March 4, 2026 · Undeclared allergen ingredient (Wheat and Sesame)