Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,527 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,527 in last 12 months

Showing 3358133600 of 52,647 recalls

Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 7, 2016· Pfizer Inc.

Recalled Item: LEVOXYL(R) (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...

The Issue: Superpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 7, 2016· Cincinnati Sub-Zero Products Inc

Recalled Item: The Hemotherm 400CE 115v Recalled by Cincinnati Sub-Zero Products Inc Due to...

The Issue: The device may not maintain water flow or temperature control.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Helena Laboratories, Inc.

Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...

The Issue: Due to a customer experiencing complaints on bone fraction of assay not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 7, 2016· Tosoh Bioscience, Inc.

Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...

The Issue: The device defect associated with this recall may result in HbA1c values...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Bayer Healthcare

Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...

The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Becton Dickinson & Company

Recalled Item: BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is Recalled by...

The Issue: BD is conducting a voluntary product recall of the BD Spinal Anesthesia...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: TENNIS ELBOW SUPPORT Recalled by DeRoyal Industries Inc Due to DeRoyal...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: PNEUGEL(R) TENNIS ELBOW STRAP Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems...

The Issue: Firm received reports about "acquisition errors" and the deterioration of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 4, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Amoxicillin for Oral suspension Recalled by West-Ward Pharmaceuticals Corp....

The Issue: Labeling: Label Error on Declared Strength: Some bottles miss a color coded...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodNovember 4, 2016· OLMA-XXI INC.

Recalled Item: Premium Norwegian Salmon Recalled by OLMA-XXI INC. Due to Potential Listeria...

The Issue: Products have the potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2016· OLMA-XXI INC.

Recalled Item: SALMON Recalled by OLMA-XXI INC. Due to Potential Listeria Contamination

The Issue: Products have the potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 4, 2016· Thayer Intellectual Property, Inc.

Recalled Item: MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a Recalled...

The Issue: The firm failed to notify current customers of IFU update/warning. During a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 3, 2016· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: OOS results for known compound.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 3, 2016· Voco GmbH

Recalled Item: VOCO Futurabond M+ adhesive Recalled by Voco GmbH Due to Labeling mix-up:...

The Issue: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...

The Issue: GE Healthcare has become aware of a potential safety issue where certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· Olympus Corporation of the Americas

Recalled Item: HF Cable WA00014A Recalled by Olympus Corporation of the Americas Due to...

The Issue: Software malfunction that results in incorrect generation or display of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· Terumo BCT, Inc.

Recalled Item: Adiprep Adipose Transfer System. Product Codes: 51431 Recalled by Terumo...

The Issue: Terumo BCT announces a voluntary field action for the Harvest : Adiprep...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· Elekta, Inc.

Recalled Item: Monaco RTP System Recalled by Elekta, Inc. Due to Incorrect Dose when using...

The Issue: Incorrect Dose when using the reset function.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing