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.

49,677 total recalls
2,453 in last 12 months

Showing 2670126720 of 49,677 recalls

Medical DeviceMarch 13, 2018· Keystone Dental Inc

Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...

The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...

The Issue: The firm received complaints of drill bits breaking during use with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...

The Issue: The power load floor plates which hold the ambulance cot anchors in place...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Zimmer Biomet, Inc.

Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...

The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ II Plus 6-Acetylmorphine Catalog # for 1000 mL: Recalled by...

The Issue: Incorrect calibrator level listed in qualitative calibration steps

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C3 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Ohio Medical Corporation

Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...

The Issue: Final quality control testing was not completed before the devices were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ II Plus 6-Acetyl morphine Catalog # for 28 Recalled by Siemens...

The Issue: Incorrect calibrator level listed in qualitative calibration steps

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 12, 2018· CooperSurgical, Inc.

Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...

The Issue: Products have been packaged with the wrong Trocar length type.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugMarch 9, 2018· Akorn, Inc.

Recalled Item: Triamcinolone Acetonide Lotion Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 9, 2018· Alva-Amco Pharmacal Companies., Inc.

Recalled Item: Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal Recalled by...

The Issue: Subpotent Drug: The product has failed to maintain its label claim of coal...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodMarch 9, 2018· Avalon Packaging

Recalled Item: NXTGEN Botanicals Recalled by Avalon Packaging Due to Potential Salmonella...

The Issue: Avalon Packaging is recalling NXTGEN Kratom because of the potential for...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 8, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Clocortolone Pivalate Cream Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Stability Specifications:Out-of-specification results observed for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Sermorelin Acetate Recalled by American Pharmaceutical Ingredients LLC Due...

The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Oxytocin USP Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: Stability Data Does Not Support Expiry: Stability data from manufacturer...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMarch 6, 2018· Piggie Park Enterprises Inc

Recalled Item: Maurice's Honey Southern Gold BBQ Sauce Recalled by Piggie Park Enterprises...

The Issue: Undeclared soy and wheat ingredients

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 5, 2018· Kodiak Cakes, LLC

Recalled Item: Kodiak Cakes Recalled by Kodiak Cakes, LLC Due to The frozen waffle product...

The Issue: The frozen waffle product contains whey but fails to declare the major food...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund