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. 2,574 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,574 in last 12 months

Showing 1970119720 of 29,284 recalls

Medical DeviceOctober 15, 2016· Natus Manufacturing Limited

Recalled Item: Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Recalled...

The Issue: The fuse blows during initial power up or after a period of time. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Reshape Medical Inc

Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...

The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Covidien LLC

Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...

The Issue: Sterility of the outer surface of the container compromised due to packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance ICT SP Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray system Recalled by Philips...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 13, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-ray system Recalled by Philips Medical...

The Issue: The product label does not include the correct current rating.

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

Class III — Low RiskOngoing
Medical DeviceOctober 12, 2016· Bausch & Lomb, Inc.

Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...

The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Alere San Diego, Inc.

Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...

The Issue: Encoded with incorrect ranges that are not consistent with the ranges...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Baxter Healthcare Corp.

Recalled Item: GAMBRO Capillary Dialyzer Recalled by Baxter Healthcare Corp. Due to...

The Issue: Potential presence of particulate matter on the blood side of the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: Radiation Therapy Treatment Planning System Product Usage: RayStation is a...

The Issue: An error may occur with the display of dose computed on images other than...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· Abbott Laboratories

Recalled Item: ARCHITECT Lactic Acid Part # 09D891T21 The Lactic Acid assay Recalled by...

The Issue: Abbott has identified negative interference from the drug N-Acetyl Cysteine...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· Zimmer Biomet, Inc.

Recalled Item: ROSA Brain Recalled by Zimmer Biomet, Inc. Due to Complaint of the head...

The Issue: Complaint of the head holder connector locking up mechanically when tightened.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: RF MultiGen¿ Recalled by Stryker Instruments Div. of Stryker Corporation Due...

The Issue: Stryker Instruments is voluntarily recalling the Care...

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

Class III — Low RiskOngoing