Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,653 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,653 in last 12 months

Showing 2478124800 of 29,496 recalls

Medical DeviceJuly 11, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management....

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: Tibila Insert UC 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· Baxter Healthcare Corporation

Recalled Item: FlowCOUPLER. An implantable device that is used to detect blood Recalled by...

The Issue: Baxter Healthcare is recalling the FlowCOUPLER Device because there is a...

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 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 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· 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· 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 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 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: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

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· Smiths Medical ASD, Inc.

Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

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· 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· Smiths Medical ASD, Inc.

Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

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· Smiths Medical ASD, Inc.

Recalled Item: H4052 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· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...

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