Product Recalls in Utah

Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,425 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,425 in last 12 months

Showing 3626136280 of 49,677 recalls

Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre NovaSil Silicone Single Lumen Embolectomy Catheter 6F 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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Civco Medical Instruments Co. Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· Cook Inc.

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.

Class II — Potential Health HazardOngoing
DrugOctober 20, 2015· Teva Pharmaceutical Industries

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.

Class III — Low RiskOngoing
Refund
FoodOctober 20, 2015· Eastland Food Corporation

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.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 20, 2015· Ameditech Inc

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.

Class II — Potential Health HazardOngoing