Product Recalls in District of Columbia

Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,411 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,411 in last 12 months

Showing 4144141460 of 47,654 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· 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· 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 6, 2014· Boston Scientific Corporation

Recalled Item: Atlantis PV Recalled by Boston Scientific Corporation Due to Reports of...

The Issue: Reports of physicians experiencing inability to pass a 0.035" guidewire...

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

Class II — Potential Health HazardOngoing
DrugJanuary 3, 2014· Dr. Reddy's Laboratories, Inc.

Recalled Item: a) Walgreens Lansoprazole Delayed Release Capsules Recalled by Dr. Reddy's...

The Issue: Microbial Contamination of Non-Sterile Products: Out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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
DrugJanuary 2, 2014· Pfizer Inc.

Recalled Item: Zithromax (azithromycin for injection) Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Pfizer is recalling certain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
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
DrugDecember 27, 2013· Mangiacotti

Recalled Item: Mangiacotti - Pomegranate Hand Sanitizer Spray Recalled by Mangiacotti Due...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund