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. 2,631 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,631 in last 12 months

Showing 1694116960 of 29,284 recalls

Medical DeviceFebruary 7, 2018· Life Technologies Corporation

Recalled Item: Human Fetal Hemoglobin (HBF-1) FITC Conjugate Recalled by Life Technologies...

The Issue: Three lots of Human Fetal Hemoglobin FITC Conjugate are displaying high...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2018· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2018· GETINGE US SALES LLC

Recalled Item: VOLISTA StandOP Surgical Light Recalled by GETINGE US SALES LLC Due to The...

The Issue: The manufacturer received complaints indicating that the device's central...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2018· Medela Inc

Recalled Item: Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Recalled...

The Issue: Device may display a battery missing error.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2018· Halyard Health, Inc

Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...

The Issue: Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2018· Baxter Healthcare Corporation

Recalled Item: Sterile EXACTAMED Oral Dispenser Recalled by Baxter Healthcare Corporation...

The Issue: Affected lot of 5 mL oral dispensers was packaged in individual pouches that...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 14 cm (5.5") Appx 0.27 ml Recalled by ICU Medical, Inc. Due to The infusion...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2018· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave¿ Clear Recalled by ICU...

The Issue: The infusion sets were manufactured with an incorrect spin collar.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 500 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Signature Orthopedics Pty Limited

Recalled Item: Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature...

The Issue: This recall has been identified due to the batch being mislabeled, with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Dako North America Inc.

Recalled Item: PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to Recalled by Dako...

The Issue: To correct the kit's instructions for use as the storage time for gastric...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Merit Medical Systems, Inc.

Recalled Item: 1mL Medallion Syringes Are used to inject fluids into Recalled by Merit...

The Issue: Supplier manufacturing defect with the syringe plunger tip.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· 3M Company - Health Care Business

Recalled Item: 3M Surgical Clipper Professional 9681 Recalled by 3M Company - Health Care...

The Issue: Failure to follow proper charging practices can result in lithium-ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans Syringe Fill 360 Recalled by Shippert Medical Technologies Due...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing