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 35921–35940 of 47,654 recalls
Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...
The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crystal Farms Simply Potatoes Shredded Hash Browns packaged as individual...
The Issue: Product may contain small slivers of shredded golf ball.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...
The Issue: Crystallization; identified as calcium salt of Ketorolac
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capecitabine Tablets Recalled by Mylan Pharmaceuticals Inc Due to Failed...
The Issue: Failed Dissolution Specifications: low out-of-specification (OOS) results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization;...
The Issue: Crystallization; identified as calcium salt of Ketorolac
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydrOXYzine Hydrochloride Tablets Recalled by Qualitest Pharmaceuticals Due...
The Issue: Failed Tablet/Capsule Specifications; The identification codes on some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring...
The Issue: Potential missing segments on the display that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterococcus Screen Agar QUAD Plate Recalled by Becton Dickinson & Co. Due...
The Issue: The affected expired lots of product may have exhibited breakthrough growth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to The...
The Issue: The affected expired lots of product may have exhibited breakthrough growth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter HomeChoice and HomeChoice Pro APD systems Recalled by Baxter...
The Issue: Loud operating sounds, which was unacceptable to the end users when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are...
The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...
The Issue: Potential missing segments on the display that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for a large amount of liquid to seep through the top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or Recalled by...
The Issue: When using the CIVCO biopsy attachments in combination with the ACUSON S...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere i flu Recalled by Alere Scarborough, Inc. dba Binax, Inc. Due to Risk...
The Issue: Risk of false negative results due to microbial growth in the Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics BEA Broth with Vancomycin container type: 13x100mm tube...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics MDR Acinetobacter container type: 15x100mm monoplate...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics BEA Agar with Vancomycin container type: 15x100mm...
The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.