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. 2,629 recalls have been distributed to District of Columbia in the last 12 months.
Showing 5941–5960 of 27,451 recalls
Recalled Item: Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level...
The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abiomed 14Fr Low Profile Introducer Set Recalled by Abiomed, Inc. Due to...
The Issue: There was one complaint that the sidearm of the device detached during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers - intended to Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be Recalled by Boston...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be Recalled by...
The Issue: Manufactured with the incorrect component may result in lower power output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilling LOWSLEY PROSTATIC TRACTOR CVD Recalled by TELEFLEX LLC Due to There...
The Issue: There are incomplete pre-cleaning instructions within the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilling O'REILLY ESOPHAGEAL RETRACTOR Recalled by TELEFLEX LLC Due to There...
The Issue: There are incomplete pre-cleaning instructions within the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilling LOWSLEY PROSTATIC TRACTOR STR Recalled by TELEFLEX LLC Due to There...
The Issue: There are incomplete pre-cleaning instructions within the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...
The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.