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 2592125940 of 29,496 recalls

Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Recalled by Roche...

The Issue: Numerous complaints have been filed that leaking cobas ¿ PCR media 4.3 mL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 Recalled by...

The Issue: Complaints were received regarding Quality Control (QC) shifts with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic GRAFTON (R) DBM Recalled by Medtronic Sofamor Danek USA Inc Due to...

The Issue: Product was labeled as being measured as 2.5 cm x 10 cm, but contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...

The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2014· Medtronic Sofamor Danek USA Inc

Recalled Item: SET SCREW RETAINING DRIVER Recalled by Medtronic Sofamor Danek USA Inc Due...

The Issue: The retaining tabs component of the Set Screw Retaining Drive may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix L/P with Echo PS 10" X 13" Product Code Recalled by Davol, Inc.,...

The Issue: Product labeling does not match product configuration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix L/P with Echo PS 6" X 8" Product Code Recalled by Davol, Inc.,...

The Issue: Product labeling does not match product configuration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 1, 2014· Abbott Point Of Care Inc.

Recalled Item: i-STAT G3+ Cartridge pH Recalled by Abbott Point Of Care Inc. Due to Abbott...

The Issue: Abbott Point of Care has determined that some individual patient results...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 30, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Neptune 2 Rover Ultra Waste Management System. Recalled by Stryker...

The Issue: The purpose of this correction is to upgrade the Neptune 2 Waste Management...

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

Class II — Potential Health HazardOngoing