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 44241–44260 of 47,654 recalls
Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...
The Issue: GE Healthcare has become aware of a potential data loss issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 25mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 35mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 30mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin Capsules USP 500 mg Recalled by Sandoz Incorporated Due to...
The Issue: Presence of Foreign Substance, Sandoz is recalling certain lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zeiss brand OPMI Pentero C Recalled by Carl Zeiss Meditec, Inc. Due to Carl...
The Issue: Carl Zeiss Meditec is conducting a field corrective action for its OPMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver¿ PTX¿ Drug-Eluting Peripheral Stent - 6 mm X 80mm Recalled by Cook,...
The Issue: Cook Medical has received a small number of complaints related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver PTX Drug-Eluting Peripheral Stent Recalled by Cook, Inc. Due to Cook...
The Issue: Cook Medical has received a small number of complaints related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Constellation Vision System Pneumatic Handpiece. Indicated for both...
The Issue: Alcon is conducting a Medical Device Removal for the Constellation Pneumatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron LX System(s) and UniCel DxC 600/800 System(s) Lactate Reagent...
The Issue: Beckman Coulter initiated the recall for the Lactate Assay (LACT) Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an Recalled by Ziemer Usa...
The Issue: A defect in the controller board can lead to the condenser to the video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended...
The Issue: Bard Peripheral Vascular (BPV) has confirmed that some devices with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The Recalled by...
The Issue: The firm initiated recall of Alere" hCG Combo Cassette (20/10 mIU/mL) kit PN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The firm is recalling all lots of sterile products compounded Recalled by...
The Issue: Lack of Assurance of Sterility: The recall is being initiated due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG (Lyophilized) Stock # 21714 Recalled by NuVision Pharmacy, Inc. Due to...
The Issue: Lack of Assurance of Sterility: The recall is being initiated due to a lack...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin/GHRP-6 Recalled by NuVision Pharmacy, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: The recall is being initiated due to a lack...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Free Form Amino Acids L-Arginine 7 L-Ornithine Complex With Alpha-Lipoic...
The Issue: Nexgen Pharma is recalling a certain lot of dietary supplement L-Arginine...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Synthes Hand Switch - Electric Pen Drive Recalled by Synthes USA HQ, Inc....
The Issue: Synthes received a complaint from a customer in which the Hand Switch for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray systems Product Usage: The Brilliance CT 64...
The Issue: Philips Healthcare received reports from the field that certain Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris Recalled by...
The Issue: The firm is recalling these power cables due to a latent design reliability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.