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. 2,495 recalls have been distributed to Utah in the last 12 months.
Showing 20961–20980 of 28,579 recalls
Recalled Item: Product 70 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LPS-FLEX Option Femoral NexGen LPS-FLEX Precoat Femoral prosthesis...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 72 consists of all product code: JDI and same Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 24 consists of all product under product code: HRS Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT 12/14 COCR prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 44 consists of all product under product code: HWC Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Microsystems (Schweiz) Ag. The common name of the device Recalled by...
The Issue: An electronic component of the Leica M525 OH4 and Leica M720 OH5 surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 25 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 48 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 12 consists of all product under product code JDI Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 31 consists of all product under product code: KTT Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 29 consists of all product under product code: LPHand Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LPS Flex Option Femoral NexGen LPS Flex Precoat Femoral prosthesis...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 52 consists of product code: HWC and same usage: Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 18 consists of all product under product code: HWC Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 5 consists of all products under product code HWC Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 28 consists of all product under product code: JDI Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 51 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 36 consists of all product under product code: HSB Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 17 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.