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. 1,718 recalls have been distributed to District of Columbia in the last 12 months.
Showing 34661–34680 of 47,654 recalls
Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 4F Recalled by LeMaitre Vascular,...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 4F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 3F Recalled by LeMaitre Vascular,...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 2F Recalled by...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 6F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 5F Plus Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 5F Recalled by LeMaitre Vascular,...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 7F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Tracking Bracket Starter Kit Recalled by Civco Medical Instruments Co....
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Sales Demo Kit. Large Gauge Infiniti Plus Recalled by Civco Medical...
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Needle Guide Starter Kit Recalled by Civco Medical Instruments Co....
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Infiniti Plus Needle Guide Recalled by Civco Medical Instruments Co....
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg Recalled by...
The Issue: Labeling: Incorrect or Missing Lot AND/OR Exp Date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maesri Brand Shrimp Powder Recalled by Eastland Food Corporation Due to The...
The Issue: The New York Department of Agriculture and Markets notified Eastland Food...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 10-Panel Pipette Drug Screen Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLIA RDTC 12-Panel Cup and CLIA RDTC 12-Panel Cup (w/Adulteration) Recalled...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart 11 Test Cup Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMO FISHER 6 DRUG CASSETTE Recalled by Ameditech Inc Due to Ameditech is...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.