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. 2,715 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,715 in last 12 months

Showing 67016720 of 29,284 recalls

Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Double Swivel Elbow Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Smiths Medical ASD Inc.

Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...

The Issue: DuraLife devices instructions for cleaning and sterilization have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...

The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) Recalled by CareFusion 303, Inc. Due to...

The Issue: Automated dispensing cabinet software is experiencing: 1) ES device download...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Infinity M300 and M300+ Recalled by Draeger Medical Systems, Inc....

The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Infinity CentralStation (ICS) Recalled by Draeger Medical Systems,...

The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2023· GRAMERCY EXTREMITY ORTHOPEDICS

Recalled Item: GEO Instrument Kit for EPS Plate Recalled by GRAMERCY EXTREMITY ORTHOPEDICS...

The Issue: Instrument Kits for EPS plates may contain drill guides with incorrect drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2023· SD Biosensor, Inc.

Recalled Item: Pilot COVID-19 At-Home Test Recalled by SD Biosensor, Inc. Due to The liquid...

The Issue: The liquid buffer component in the affected test kit lots was determined to...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 31, 2023· Greiner Bio-One North America, Inc.

Recalled Item: greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA Recalled by Greiner Bio-One...

The Issue: Some of the tubes may be incorrectly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2023· Baxter Healthcare Corporation

Recalled Item: Hill-Rom pro+ mattress Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential for mattress cover damage (delamination) which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2023· Apothecary Products, LLC

Recalled Item: Eye and Ear Dropper Recalled by Apothecary Products, LLC Due to Potential...

The Issue: Potential for glass dropper to have glass particulate on the outside surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2023· Apothecary Products, LLC

Recalled Item: Medicine Dropper Recalled by Apothecary Products, LLC Due to Potential for...

The Issue: Potential for glass dropper to have glass particulate on the outside surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs Recalled by...

The Issue: The case and each (i.e. packet) labels for the DYND3000xxP series do not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2023· Surgical Innovations Ltd

Recalled Item: YelloPort Elite Recalled by Surgical Innovations Ltd Due to Optical Trocars...

The Issue: Optical Trocars sterility assurance can not be guaranteed

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2023· Surgical Innovations Ltd

Recalled Item: YelloPort Elite Recalled by Surgical Innovations Ltd Due to Optical Trocars...

The Issue: Optical Trocars sterility assurance can not be guaranteed

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2023· IMMUNDIAGNOSTIK, Inc

Recalled Item: Immundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended...

The Issue: Marketed without a 510k

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2023· Technidata S.A.

Recalled Item: TDHisto/Cyto - A software product used for managing medical information...

The Issue: In a specific use case, when printing labels for slides, some labels may...

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

Class II — Potential Health HazardOngoing