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. 2,482 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,482 in last 12 months

Showing 2188121900 of 49,677 recalls

Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...

The Issue: Supplemental information provided with devices may indicate that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: LSB Style Anchor Bolt. Labeled with the following parts: 13mm Recalled by...

The Issue: On June 12, 2019 Ad-Tech was made aware that on three different occasions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Howmedica Osteonics Corp.

Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...

The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...

The Issue: The products' cut, coagulate, or blend function may not operate with the use...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2019· Bausch & Lomb

Recalled Item: Lotemax (loteprednol etabonate ophthalmic gel 0.5%) Recalled by Bausch &...

The Issue: Failed Stability Specifications: Out of specification for viscosity.

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2019· Intuitive Surgical, Inc.

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

The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...

The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: Battery short-run times and unanticipated stoppage may be due to user not...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...

The Issue: If battery maintenance is not performed appropriately, the battery may...

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

Class I — Serious Health HazardOngoing
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2019· Sprout's Farmers Market

Recalled Item: Sprouts Farmers Market Cut Leaf Spinach Recalled by Sprout's Farmers Market...

The Issue: Testing revealed the presence of Listeria monocytogenes in the frozen spinach

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 14, 2019· Sprout's Farmers Market

Recalled Item: Sprouts Farmers Market Organic Cut Leaf Spinach Recalled by Sprout's Farmers...

The Issue: Testing revealed the presence of Listeria monocytogenes in the frozen spinach

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 14, 2019· TELEFLEX-MORRISVILLE

Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by...

The Issue: Device vented gas below the stated pressure.

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

Class I — Serious Health HazardOngoing