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. 2,542 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,542 in last 12 months

Showing 2458124600 of 29,284 recalls

Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Daily Dressing Advanced 3-in-1 Hydrogel Recalled by Amerx Health...

The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2014· Ortho Development Corporation

Recalled Item: Tibila Insert CK Recalled by Ortho Development Corporation Due to Ortho...

The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2014· Medical Positioning Inc

Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...

The Issue: Excessive weight on the table will cause tables with the affected component...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2014· Teleflex Medical

Recalled Item: RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe Recalled by...

The Issue: Labeling error: The manufacturing date is the same as the expiration date....

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

Class III — Low RiskOngoing
Medical DeviceJuly 10, 2014· Medical Positioning Inc

Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...

The Issue: Excessive weight on the table will cause tables with the affected component...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2014· Medical Positioning Inc

Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...

The Issue: Excessive weight on the table will cause tables with the affected component...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2014· Medical Positioning Inc

Recalled Item: Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section...

The Issue: Excessive weight on the table will cause tables with the affected component...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Nanosphere, Inc.

Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...

The Issue: Nanosphere Inc. has recently determined through four customer complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...

The Issue: The temperature probe does not properly connect to the temperature port.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Richard Wolf Medical Instruments Corp.

Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...

The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Teleflex Medical

Recalled Item: Hudson RCI Recalled by Teleflex Medical Due to The temperature probe does...

The Issue: The temperature probe does not properly connect to the temperature port.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2014· Carestream Health, Inc.

Recalled Item: Kodak DirectView DR 7500 Diagnostic X-Ray System Product Usage: The Recalled...

The Issue: An on-site evaluation of the equipment parts that attach the Beta Assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2014· Gyrus Medical, Inc

Recalled Item: Gyrus ACMI Falope-Ring Dilator Recalled by Gyrus Medical, Inc Due to...

The Issue: Falope-Ring Dilator for Reusable Falope-Ring Band Applicators have been sold...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Stryker Spine

Recalled Item: Specialty Aria Inserter Recalled by Stryker Spine Due to Stryker has...

The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Stryker Spine

Recalled Item: Stryker Aria Implant Inserter Recalled by Stryker Spine Due to Stryker has...

The Issue: Stryker has initiated the recall of its Aria Standard and Specialty Implant...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Innovasis, Inc

Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling

The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...

The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...

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

Class II — Potential Health HazardOngoing