Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 2504125060 of 28,641 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· Infantino LLC

Recalled Item: Infantino Squeeze & Teethe Monkey Recalled by Infantino LLC Due to Infantino...

The Issue: Infantino initiated this voluntary recall of all lots of Infantino Squeeze &...

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· 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 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 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 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
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
Medical DeviceDecember 27, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: The Gaymar Medi-Therm device provides a means of regulating patient Recalled...

The Issue: Stryker Medical has identified that on some units of the MTA7900, there is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. The...

The Issue: GE Healthcare has recently become aware of potential safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2013· Vital Signs Colorado Inc.

Recalled Item: Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for...

The Issue: A circuit in use was occluded by a blue port cap that was inadvertently...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2013· Carestream Health, Inc.

Recalled Item: KODAK DirectView DR 7500 Dual Detector System Recalled by Carestream Health,...

The Issue: Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 183 cm (72") Smallbore Quadfuse Ext Set w/4 NanoClave¿ (Yellow Recalled by...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.37 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing