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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.
Showing 47081–47100 of 47,654 recalls
Recalled Item: Depuy Spine Side Fire Needles 11G X 4IN Recalled by DePuy Mitek, Inc., a...
The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Depuy Spine Side Fire Needles 13G X 4IN Side-Fire Needle Recalled by DePuy...
The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R)...
The Issue: Lidstock of product does not contain chlorhexidine contraindication and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeosa (norethindrone and ethinyl estradiol tablets USP Recalled by Teva...
The Issue: Impurities/Degradation: This recall is being carried out due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Octreotide Acetate Injection Recalled by Ben Venue Laboratories Inc Due to...
The Issue: Short Fill: These products are being recalled because there is potential...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Midazolam HCl Injection Recalled by Ben Venue Laboratories Inc Due to Short...
The Issue: Short Fill: These products are being recalled because there is potential...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/STD Recalled by Nidek Medical Products Inc...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical MARK5 NUVO 8 /OCSI Recalled by Nidek Medical Products Inc Due...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical MARK5 NUVO 8 STD Recalled by Nidek Medical Products Inc Due to...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical M5C5/ MARK5 NUVO/OCSI Recalled by Nidek Medical Products Inc...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 525 OCSI Recalled by Nidek Medical Products...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical MARK5 NUVO / M5C5 Recalled by Nidek Medical Products Inc Due...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 925 OCSI Recalled by Nidek Medical Products...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Medical NUVO LITE MODEL 520 STD Recalled by Nidek Medical Products Inc...
The Issue: Capacitor failure may result in a fire hazard and loss of supplemental oxygen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dorzolamide HCI/Timolol Maleate Ophthalmic Solution 22.3mg/6.8mg per mL...
The Issue: Presence of Particulate Matter: Lots identified in this recall notification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Uroskop Access. Fluoroscopic Recalled by Siemens Medical Solutions...
The Issue: Siemens has discovered a possible hazard to patients or hospital personnel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray...
The Issue: During regular product monitoring, firm became aware of a potential issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor...
The Issue: The design of the spring clip for the jaw assembly was updated in March 2011...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral Recalled...
The Issue: The design of the spring clip for the jaw assembly was updated in March 2011...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.