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. 2,453 recalls have been distributed to Utah in the last 12 months.
Showing 27741–27760 of 28,579 recalls
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX Plus High Speed Compounder System Recalled by Baxter Healthcare...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oto Ease by Westone Recalled by Westone Laboratories, Inc. Due to Westone is...
The Issue: Westone is recalling all Oto Ease ear lubricant in all packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX 3+3 Compounder with Accusource Monitoring System Recalled by Baxter...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...
The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage TOX Drug Screen 9 Panel Recalled by Alere San Diego, Inc. Due...
The Issue: Alere San Diego is recalling Alere Triage TOX Drug Screen because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a number of potential issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Adult Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...
The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Premium Small Child Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Rescue Med Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Resuscitator Recalled by Ventlab Corporation Due to Possible volume...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034...
The Issue: When doing a 3 Dimensional Rotational Angiography (3DRA) the 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stat-Check Resuscitator Recalled by Ventlab Corporation Due to Possible...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V*Care Resuscitator Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.