Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,540 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,540 in last 12 months

Showing 65416560 of 48,219 recalls

Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7270 / Integra¿ Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INS7250 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : 31156 / COMBO KIT CONTAINS INS-8301 Recalled by Integra LifeSciences Corp....

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: INS7280 / Integra¿ Cranial Access Kit. For access to the Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INSHITHND / Integra¿ Cranial access kit (without Prep Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INSHITH / Integra¿ Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· Integra LifeSciences Corp.

Recalled Item: : INSHITHRZN / Integra Cranial Access Kit. For access Recalled by Integra...

The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2024· W.L. Gore & Associates, Inc.

Recalled Item: GORE VIABIL Short Wire Biliary Endoprosthesis Recalled by W.L. Gore &...

The Issue: Devices without transmural drainage holes may be mislabeled as devices with...

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

Class II — Potential Health HazardOngoing
FoodJanuary 18, 2024· UNFI General Corporate

Recalled Item: Woodstock 5 Grain Cereal. Oats Recalled by UNFI General Corporate Due to The...

The Issue: The ingredient Triticale is not identified as wheat.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Glimepiride Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Misprint on tablet

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Glimepiride Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Misprint on tablet

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lurasidone Hydrochloride Tablets 60mg Recalled by SUN PHARMACEUTICAL...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Zolpidem Tartrate Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Mesalamine Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cinacalcet Tablets 60mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Lurasidone Hydrochloride Tablets 120mg Recalled by SUN PHARMACEUTICAL...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Niacin Extended-Release Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Niacin Extended-Release Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 80 mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund