Recalls in Massachusetts (page 32)
3965 recalls.
- Icosapent Ethyl Capsules recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported March 18, 2026 · Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient. - 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... - Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal... recall (Altruan GmbH)
Medical deviceClass IIReported March 18, 2026 · Product not cleared by the FDA. - Clearest Strep-A Cassette Test. Test to determine the presence of group A streptococci recall (Altruan GmbH)
Medical deviceClass IIReported March 18, 2026 · Product not cleared by the FDA. - Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic... recall (Altruan GmbH)
Medical deviceClass IIReported March 18, 2026 · Product not cleared by the FDA. - 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... - EndoVive Safety PEG Kit recall (Boston Scientific Corporation)
Medical deviceClass IIReported March 18, 2026 · Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of... - 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. - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - 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. - IBA Proton Therapy System - PROTEUS 235 recall (Ion Beam Applications S.A.)
Medical deviceClass IIReported March 18, 2026 · It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS... - 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. - LFTE USA Recalls Playground Swing Set Seats Due to Fall Hazard
Consumer productReported March 13, 2026 · The rivets used to support the swing seat can fail, posing a fall hazard to children. - 17 Stories Furniture 14-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by Hong Kong Baojia International
Consumer productReported March 12, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - LIVEHOM 11-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Sold on Amazon by Simplehome
Consumer productReported March 12, 2026 · The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or... - ProRider Recalls Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
Consumer productReported March 12, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional... - Stoney Games Recalls Kluster Magnet Chess Games Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
Consumer productReported March 12, 2026 · The recalled magnet games violate the mandatory standard for toys because they contain loose high-powered magnets that fit within CPSC's small parts cylinder... - Gelsoft Plus recall (Vascutek, Ltd.)
Medical deviceClass IIReported March 11, 2026 · Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life. Device expiry... - 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. - Amnesteem recall (MYLAN PHARMACEUTICALS INC)
DrugClass IIReported March 11, 2026 · Failed Dissolution Specifications - Sodium Iodide recall (Radnostix)
DrugClass IIReported March 11, 2026 · Presence of Particulate Matter: Due to production issues - MAXIMUM recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - MAXIMUM recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - FIVE-STAR recall (HTO Nevada Inc. dba Kirkman)
DrugClass IIReported March 11, 2026 · Stability Data Does Not Support Expiry Date. - Product label: Temozolomide Capsules recall (Rising Pharma Holding, Inc.)
DrugClass IIReported March 11, 2026 · Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing - Midodrine Hydrochloride Tablets recall (The Harvard Drug Group LLC)
DrugClass IIReported March 11, 2026 · Defective container; inadequately sealed blister packaging. - Nilotinib Capsules recall (Cipla USA, Inc.)
DrugClass IIIReported March 11, 2026 · Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection... - Nilotinib Capsules recall (Cipla USA, Inc.)
DrugClass IIIReported March 11, 2026 · Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection... - Semaglutide recall (Harbin Jixianglong Biotech Co., Ltd.)
DrugClass IIReported March 11, 2026 · CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution - Semaglutide recall (Harbin Jixianglong Biotech Co., Ltd.)
DrugClass IIReported March 11, 2026 · CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution - 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: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S ... recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported March 11, 2026 · The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values. - 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.