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.
Showing 35821–35840 of 49,677 recalls
Recalled Item: Hazelnut Raw Cacao - Sprouted Hazelnut Spread. Product is packaged in glass...
The Issue: Hazelnut Raw Cacao - Sprouted Hazelnut Spread is recalled because it has the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...
The Issue: The item was recalled due to an increased user/patient risk of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for...
The Issue: The hardware that holds the VESA plate and the display interface / monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set Recalled by...
The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set Recalled by...
The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS-500 Scope Warmer Recalled by JosNoe Medical, Inc. Due to Damage to...
The Issue: Damage to package seals potentially compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Coban Self-Adherent Wrap Shipper carton label identified the product...
The Issue: Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHES Recalled by Synthes (USA) Products LLC Due to The 13.5mm Medullary...
The Issue: The 13.5mm Medullary Reamer head, lot #F-17180, is etched as dimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CNSystems TASK FORCE MONITOR 3040i Recalled by Partners In Medicine Llc Due...
The Issue: Device non-conformity which may lead to an incorrect oscillometric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 20 Recalled by Beckman Coulter...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 33 Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 21 Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 34 Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.