Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 983 recalls have been distributed to Virginia in the last 12 months.
Showing 39001–39020 of 53,829 recalls
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: Cook Medical CXI Support Catheter 2.6FR curved catheter and 4.0FR Recalled...
The Issue: Cook Medical has received six product complaints associated with reports of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: Presence of Foreign Tablets/Capsules: one foreign capsule identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION Recalled by Vintage...
The Issue: Failed Stability Specifications: Out of Specification results obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 11 Panel Dip Card (OPI 2000) 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.
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: DrugCheck Pipette 10 Drug Test 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.