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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 2844128460 of 29,284 recalls

Medical DeviceJuly 11, 2012· Straumann USA, LLC

Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...

The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Adult Resuscitator Recalled by Ventlab Corporation Due to Possible volume...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2012· Ventlab Corporation

Recalled Item: Ventlab Rescue Med Infant Resuscitator Recalled by Ventlab Corporation Due...

The Issue: Possible volume leakage through the inlet valve during compressions of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2012· GE Healthcare, LLC

Recalled Item: Optima XR220amx Mobile general purpose radiographic imaging of the human...

The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2012· Berchtold Corp.

Recalled Item: Chromovision High Definition (HD) Wireless Camera Recalled by Berchtold...

The Issue: Defective camera: There is a possibility that the connection of the wires to...

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

Class III — Low RiskOngoing
Medical DeviceJuly 10, 2012· GE Healthcare, LLC

Recalled Item: Optima XR200amx. Mobile general purpose radiographic imaging of the human...

The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2012· AGFA Corp.

Recalled Item: IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component...

The Issue: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage:...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Sentec AG

Recalled Item: SenTec Recalled by Sentec AG Due to SenTec is recalling a number of V-Sign"2...

The Issue: SenTec is recalling a number of V-Sign"2 Sensors due to a problem regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: Recalled...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Iris Diagnostics

Recalled Item: IRISpec" CA/CB two-part urine chemistry control twin set Recalled by Iris...

The Issue: The firm recalled after it received complaints of IRISpec CA/CB two part...

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

Class III — Low RiskOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage:...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage:...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2012· Baxter Healthcare Renal Div

Recalled Item: Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic...

The Issue: Baxter discovered that a Baxter technical service representative was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2012· FMS, Finapres Medical Systems BV

Recalled Item: Finapres Medical Systems Portapres with NiMh battery pack Product Usage:...

The Issue: Battery may become hot and leak

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2012· Beckman Coulter Inc.

Recalled Item: Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i Recalled by Beckman...

The Issue: The recall was initiated because Beckman Coulter has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Kimberly-Clark Corporation

Recalled Item: ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is...

The Issue: Package seam of some units may not remain properly sealed to ensure the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Radiometer America Inc

Recalled Item: ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer Recalled by...

The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...

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

Class II — Potential Health HazardOngoing