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. 2,477 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,477 in last 12 months

Showing 4234142360 of 52,647 recalls

Medical DeviceNovember 20, 2014· Philips Medical Systems, Inc.

Recalled Item: Lithium Polymer Fiber Optic Module Batteries used in the Intera Recalled by...

The Issue: VCG battery ignited in a VCG unit when recharging.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Phadia US Inc

Recalled Item: Phadia 1000 Instrument (introduced as UniCAP 1000) Recalled by Phadia US Inc...

The Issue: During an investigation of instrument logs it was determined that In...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended Recalled...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 13/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 13/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/60 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Boston Scientific Corp

Recalled Item: IntellaMap Orion High Resolution Mapping Catheter Recalled by Boston...

The Issue: Some IntellaMap Orion High Resolution Mapping Catheters are exhibiting a...

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2014· American Health Packaging

Recalled Item: Mercaptopurine Tablets Recalled by American Health Packaging Due to Failed...

The Issue: Failed USP Dissolution Test Requirements: This sub-recall is in response to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 19, 2014· Philips Electronics North America Corporation

Recalled Item: ECG Out Cable Recalled by Philips Electronics North America Corporation Due...

The Issue: When a Philips monitor/defibrillator is receiving an ECG signal from an...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models:M3535A Recalled by...

The Issue: MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A...

The Issue: 1. Device will perform the weekly automated tests hourly, which could cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue TcG10 Recalled by Philips Medical Systems, Inc. Due to...

The Issue: Philips has discovered that the Instructions for Use (IFU) for the...

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

Class II — Potential Health HazardOngoing