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. 2,677 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,677 in last 12 months

Showing 1360113620 of 29,284 recalls

Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK TNA 2 Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 1 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max MRSA Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Vaginal Panel Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 2 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max CT/GC/TV Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Cdiff EU Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max GC RT PCR Assay Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Parasite Panel EU Recalled by Becton Dickinson & Co. Due...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 2 USA Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Bacterial Panel EU Recalled by Becton Dickinson & Co. Due...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max MRSA XT Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· TeDan Surgical Innovations LLC

Recalled Item: Fukushima suction tubes Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: There was incorrect raw material used in the production of the identified lot.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· Luminex Molecular Diagnostics

Recalled Item: xTAG Respiratory Viral Panel (RVP): Box Label: xTAG RVP (Respiratory...

The Issue: The Assay may give a false negative result when detecting and subtyping...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Model # M3535A - Product Usage: The...

The Issue: Non-conforming devices are identified, which may not have been included in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 05031656160 Recalled by Roche...

The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Elecsys Anti-CCP Immunoassay Catalog # 07251670190 Recalled by Roche...

The Issue: Performance issues with certain lots of the Elecsys Anti-CCP assay on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· Philips North America, LLC

Recalled Item: Philips Azurion systems with software version R1.2 -Interventional...

The Issue: The cold restart of Azurion R1.2 systems may take up to 7 minutes if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2019· ICU Medical, Inc.

Recalled Item: ICU Medical Cogent Hemodynamic Monitoring System Recalled by ICU Medical,...

The Issue: Firm identified several software issues through internal testing of its...

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

Class II — Potential Health HazardOngoing