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. 1,642 recalls have been distributed to District of Columbia in the last 12 months.
Showing 44081–44100 of 47,654 recalls
Recalled Item: Versaport Bladeless Optical Trocar With Fixation Cannula - 5mm Long Recalled...
The Issue: Seals may disengage from the cannula which may result in a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to There is evidence...
The Issue: There is evidence that an electrical short within the systems connector has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...
The Issue: Siemens has discovered through product monitoring a potential malfunction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension(R) Chemistry Wash (RD701) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics received complaints of Chemistry Wash causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach...
The Issue: Product did not reach expected sterility assurance level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadSuite software. The firm name on the label is Merge Healthcare Recalled...
The Issue: Multiple studies were missing at a customer location that never made it to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lightning ROD capsules Recalled by Chang Kwung Products Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Lightning Rod capsules are being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pure-Aid Allergy Relief Recalled by Kareway Product Inc Due to Labeling: Not...
The Issue: Labeling: Not Elsewhere Classified; foil label on immediate blister pack...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Large Tear Cross Cut Rasp 14mm x 7mm Ref. 5100-37-114 Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - ConMed Linvatec Spectrum II Suture Hook Crescent Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: -ENDOPATH ETS-Flex Articulating Endoscopic Linear Cutter Recalled by...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Turbosonics Mini-Flared ABS Tip Recalled by Surgical Instrument Service...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Acorn Bur Recalled by Surgical Instrument Service And Savings, Inc. Due to...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - ENDOPATH Resposable Bladeless Trocar Recalled by Surgical Instrument...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - ACCU-PASS Suture Shuttle Recalled by Surgical Instrument Service And...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barron Radial Vacuum Trephine (1) Complete Trephine Set 9.0mm Dia. Recalled...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Abrader Bur Recalled by Surgical Instrument Service And Savings, Inc. Due...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmonic ACE Ergonomically-Enhanced Curved Shear Recalled by Surgical...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.