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 3038130400 of 49,677 recalls

DrugApril 13, 2017· Spectrum Laboratory Products, Inc.

Recalled Item: Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP...

The Issue: CGMP Deviations: these repackaged and redistributed products are being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2017· XTANT MEDICAL INC

Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...

The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Datascope Corporation

Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...

The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...

The Issue: An extremely dusty computer can cause problems at system start, or rarely,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...

The Issue: An unexpected transient mode switch behavior was detected by Medtronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: OVATIO Models: VR 6250 Recalled by Sorin Group Italia SRL - CRF Due to Sorin...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: INTENSIA Models: VR 124 Recalled by Sorin Group Italia SRL - CRF Due to...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Biomet Microfixation, LLC

Recalled Item: Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600...

The Issue: Part of the number on the tray lid differ from the part number on the base.

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

Class II — Potential Health HazardOngoing
FoodApril 11, 2017· Jimmy's Cookies

Recalled Item: The Bakery Peanut Butter Chocolate Chunk Cookies Recalled by Jimmy's Cookies...

The Issue: The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 10, 2017· B Braun Medical Inc

Recalled Item: CytoGuard Closed Luer Connector Recalled by B Braun Medical Inc Due to B....

The Issue: B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2017· Roche Diagnostics Corporation

Recalled Item: Elecsys PreciControl Varia 3 Recalled by Roche Diagnostics Corporation Due...

The Issue: e-barcode and value sheet for PreciControl Varia contains a typographical...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2017· CooperSurgical, Inc.

Recalled Item: CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit...

The Issue: The current secondary packaging, a box, incorrectly states that the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2017· bioMerieux, Inc.

Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...

The Issue: Some anomalies have been identified during manufacturing controls.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2017· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional...

The Issue: Potential Patient Demographic Error with Blank Patient ID Field

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2017· Merge Healthcare, Inc.

Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...

The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...

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

Class II — Potential Health HazardOngoing
DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate 40 mg/mL Recalled by Isomeric Pharmacy Solution,...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate 80 mg/mL Recalled by Isomeric Pharmacy Solution,...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Phenylephrine 2.5% Recalled by Isomeric Pharmacy Solution, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund