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. 2,429 recalls have been distributed to District of Columbia in the last 12 months.
Showing 35561–35580 of 47,654 recalls
Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction Systems for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Closed Suction System for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VEPTR Vertical Expandable Prosthetic Titanium Rib Recalled by Synthes (USA)...
The Issue: The last hole on certain VEPTR Inferior Cradles may be partially formed....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Trauma Ex-Fix System (Small Recalled by Synthes (USA) Products LLC...
The Issue: Labeling changes were made related to MR conditions that align with standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...
The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets Recalled by Vintage Pharmaceuticals LLC dba Qualitest...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Wockhardt Usa Inc. Due to CGMP...
The Issue: CGMP Deviations: An FDA inspection identified inadequate investigations of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydralazine Hydrochloride Injection Recalled by Fresenius Kabi USA, LLC Due...
The Issue: Incorrect Expiration Date: The "11/06" expiration date printed on the tray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.