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. 2,495 recalls have been distributed to Utah in the last 12 months.

49,677 total recalls
2,495 in last 12 months

Showing 2040120420 of 49,677 recalls

FoodOctober 18, 2019· Cold Locker Processing LLC

Recalled Item: Kroger Wild Caught Sockeye Salmon Boneless Recalled by Cold Locker...

The Issue: Kroger Wild Caught Sockeye Salmon, Frozen, is recalled due to a potential...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 18, 2019· Capso Vision, Inc.

Recalled Item: CapsoCAM Plus Recalled by Capso Vision, Inc. Due to Capsule Endoscopy...

The Issue: Capsule Endoscopy System: a defect present in the capsule window may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· CP Medical Inc

Recalled Item: Coated PGA Undyed Polyglycolic Acid Braided Absorbable Suture Sterile EO...

The Issue: Failed to meet USP minimum average value for knot pull (tensile) strength.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· Brasseler USA I Lp

Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...

The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· Tornier, Inc

Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...

The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...

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

Class II — Potential Health HazardOngoing
DrugOctober 17, 2019· Sandoz Inc

Recalled Item: Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension...

The Issue: Labeling: Incorrect or missing package insert.

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

Class III — Low RiskOngoing
Refund
DrugOctober 17, 2019· Sandoz Inc

Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Sandoz Inc Due to...

The Issue: Labeling: Incorrect or missing package insert.

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

Class III — Low RiskOngoing
Refund
DrugOctober 17, 2019· Sandoz Inc

Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Sandoz Inc Due to...

The Issue: Labeling: Incorrect or missing package insert.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 16, 2019· CooperSurgical, Inc.

Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...

The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2019· CooperSurgical, Inc.

Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...

The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2019· CooperSurgical, Inc.

Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...

The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2019· Philips North America, LLC

Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...

The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...

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

Class II — Potential Health HazardOngoing
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Articula Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Ouch Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Connectissue Recalled by 8046255 Canada Inc. DBA Viatrexx Due to...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Hair Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Intra-Cell Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Collagen Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Lymph 1 Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-ANS/CNS Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...

The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...

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

Class II — Potential Health HazardOngoing
Refund