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.
Showing 38401–38420 of 47,654 recalls
Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mini Naan Eight (8) nann packaged in coated paper printed Recalled by fgf...
The Issue: The products were shipped without labels declaring the nutrition and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...
The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoftPath Laboratory Information System. Versions 4.3.0.8 Recalled by SCC...
The Issue: Modifications to diagnostic text may be: 1) Saved to the database but not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GETINGE 46-SERIES Medical Washer-Disinfector Recalled by Getinge...
The Issue: Getinge Disinfection AB received complaints regarding sediment residuals in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer PERSONA Tibial Articular Surface Inserter Recalled by Zimmer, Inc....
The Issue: Potential for fracture of the tip of the product. The fractured tip is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...
The Issue: While servicing a unit at a customer site, a field engineer discovered a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TactiSys Quartz Pack Recalled by St Jude Medical Due to A configuration...
The Issue: A configuration update needs to be done on TactiSys to appropriately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dacarbazine Recalled by Hospira Inc. Due to Discoloration: Reconstituted...
The Issue: Discoloration: Reconstituted solution may appear pink instead of colorless...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...
The Issue: Lack of Assurance of Sterility; leaks were observed from the bag seam and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Par Pharmaceutical Inc. Due to...
The Issue: Presence of Foreign Substance: Par Pharmaceutical, Inc. is recalling one lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Myoglobin Calibrator (MYO CAL) Recalled by Siemens...
The Issue: Dimension Vista Myoglobin Calibrator (MYO CAL) may produce a positive shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Athrosurface 40mm 13.75x31mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoject E1 Fixed needle device Recalled by Owen Mumford USA, Inc. Due to...
The Issue: The syringe carrier is missing components: a damper and spring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component Recalled by...
The Issue: Fully threaded Taper Post Fixation components not cleared for marketing in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BBL Port A Cul tubes with Swabs Sterile Pack Recalled by Becton Dickinson &...
The Issue: The products may exhibit indications of excessive oxidation. Excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carlens Bronchial Double Lumen Tube Set (Left) Sterile Recalled by Teleflex,...
The Issue: Customer complaints reporting that the cobb connector detached from the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.