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. 2,445 recalls have been distributed to District of Columbia in the last 12 months.
Showing 33061–33080 of 47,654 recalls
Recalled Item: PerioRx (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORIS (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Renovo Patch (Capsaicin Recalled by TMIG Inc Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Failed pH...
The Issue: Failed pH Specifications: Confirmed high out of specification (OOS) results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...
The Issue: Incorrect expiration date was listed on the label. Correct expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...
The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Hospira Inc. Due to Presence...
The Issue: Presence of Particulate Matter: particulate matter identified as an insect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...
The Issue: The device may have a defect in the catheter. In some instances this defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD-Retic-Count Reticulocyte Reagent System Recalled by Becton, Dickinson and...
The Issue: The carton label for one lot of BD Retic-Count Reticulocyte Reagent System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.