Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. 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 Mississippi in the last 12 months.
Showing 35521–35540 of 49,744 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: 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: 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: 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: ProScreen 10 Drug Panel Cassette Test Recalled by Ameditech Inc Due to...
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: iCup Drug Screen Cup Recalled by Ameditech Inc Due to Ameditech is recalling...
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: Micro Screen 6 Panel Cup with Adult (AU) Recalled by Ameditech Inc Due to...
The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.