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. 2,657 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,657 in last 12 months

Showing 1484114860 of 29,284 recalls

Medical DeviceJanuary 14, 2019· Teleflex Medical

Recalled Item: RUSCH CARE Premium Drain bag Recalled by Teleflex Medical Due to The device...

The Issue: The device labels are not UDI compliant. The missing UDI compliance...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 14, 2019· Arthrex, Inc.

Recalled Item: Arthrex Burr Recalled by Arthrex, Inc. Due to Devices may generate excessive...

The Issue: Devices may generate excessive heat during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2019· Shimadzu Medical Systems Usa Com

Recalled Item: SHIMADZU MobileDaRt Evolution (MX8 Version) Recalled by Shimadzu Medical...

The Issue: In these units, the brake is usually released by gripping the drive handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2019· Becton Dickinson & Co.

Recalled Item: BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use Recalled by...

The Issue: False negative results with the BD MAX Extended Enteric Bacterial Panel when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2019· Shimadzu Medical Systems Usa Com

Recalled Item: BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is...

The Issue: Normal operation of the device is to power up the device in the morning,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2019· Lin-Zhi International Inc

Recalled Item: Ethyl Alcohol Enzymatic Assay Recalled by Lin-Zhi International Inc Due to...

The Issue: Shelf life of the product may be reduced due to degradation of the assay.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 11, 2019· AAP Implantate Ag

Recalled Item: aap Implante AG Recalled by AAP Implantate Ag Due to There is the potential...

The Issue: There is the potential for the Lambotte chisel to break at the welded piece...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Bio-Rad Laboratories, Inc

Recalled Item: EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management...

The Issue: User-induced circumstances can contribute to the EVOLIS Microplate Processor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: DELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14 PushValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Karl Storz Endoscopy

Recalled Item: Insufflation tubing to be used with varies insufflator units. Recalled by...

The Issue: The sterile single-use tubing may contain higher ethylene oxide (EO)...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Feeding Tube Metric Recalled by ConvaTec, Inc Due to An internal assessment...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Forceps Blue Recalled by ConvaTec, Inc Due to An internal assessment of...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing