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 35901–35920 of 47,654 recalls
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman Recalled by...
The Issue: Bella Rosa Grated Parmesan Cheese may contain undeclared egg lysozyme.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT) Recalled...
The Issue: Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zero Xtreme High Performance Fat Burner capsules Recalled by XTREME Z...
The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iovera 155 Smart Tip Recalled by Myoscience Inc Due to The expiration date...
The Issue: The expiration date on the outer box label and the pouch label for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Base CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...
The Issue: Philips has identified four (4) software defects in the Tumor LOC software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep B Grouping Latex Recalled by Remel Inc Due to A reagent...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Processor EPX 2500 High Definition Endoscopy Recalled by Fujifilm...
The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic...
The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...
The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Acetaminophen reagents Recalled by Siemens Healthcare...
The Issue: A change in the concentration of N-acetylcysteine (NAC) that may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...
The Issue: A reagent present may produce weak or slow reactions; continued use may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.