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. 2,373 recalls have been distributed to District of Columbia in the last 12 months.
Showing 44401–44420 of 47,654 recalls
Recalled Item: Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an...
The Issue: Several complaints were recorded regarding one of the three screws driving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE 1.5T Signa HDxt Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalight 80 Model Number UVB-080 Recalled by National Biological Corp Due...
The Issue: The incorrect manual may have been packaged with this product. UVB-080...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL RecombiPlasTin 2G Recalled by Instrumentation Laboratory Co. Due to...
The Issue: Instrumentation Laboratory is recalling HemosIL RecombiPlasTin 2G (RPT2G),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neurology Dantec KEYPOINT.NET 2.20. Catalog/Part Numbers: 9031A070103...
The Issue: Alpine Biomed ApS is recalling Natus neurology Dantec KEYPOINT.NET ver. 2.20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: A single visible particulate was identified...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Endopath Electrosurgery Probe Plus II Recalled by Ethicon Endo-Surgery Inc...
The Issue: The firm is recalling the ENDOPATH Probe Plus II Shafts because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defribillator Recalled by Philips Healthcare Inc. Due...
The Issue: Device may fail to deliver defibrillation therapy in either Manual Defib or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product...
The Issue: Defibrillation Electrodes may arc/spark result in thermal damage to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glenmark Gabapentin Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Gabapentin Sodium tablets is recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Pravastatin Sodium Tablets Recalled by Glenmark Generics Inc., USA...
The Issue: Chemical Contamination: Pravastatin Sodium Tablets isbeing recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glenmark Topiramate Tablets Recalled by Glenmark Generics Inc., USA Due to...
The Issue: Chemical Contamination: Topiramate Tablets is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROFILE-V MEDTOXScan Drugs of Abuse Test System. For the rapid Recalled by...
The Issue: Review of validation information and customer complaints which indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rite Aid brand Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling
The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848...
The Issue: An LPC Fine Mesh Cassette failed to stay closed during processing operations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS PANELS Recalled by Polymer Technology Systems, Inc. Due to Internal...
The Issue: Internal investigation demonstrated under-recovery for glucose when tested...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.