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. 2,391 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,391 in last 12 months

Showing 2246122480 of 48,219 recalls

Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 10, 2019· MAJOR PHARMACEUTICALS

Recalled Item: Losartan Potassium Tablets Recalled by MAJOR PHARMACEUTICALS Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2019· McGuff Compounding Pharmacy Services, Inc.

Recalled Item: Lipoic Acid Injection (aka Alpha Lipoic Acid or Thioctic Acid) Recalled by...

The Issue: Presence of Particulate Matter: filmy/cloudy particulate observed in vial.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC50 Government Bundle Recalled by Philips North America, LLC Due...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Forceps Blue Recalled by ConvaTec, Inc Due to An internal assessment of...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC20 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 w/o trolley Government Bundle Recalled by Philips North...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Feeding Tube Metric Recalled by ConvaTec, Inc Due to An internal assessment...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC50 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2019· Acuity Surgical Devices, LLC

Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...

The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2019· Acuity Surgical Devices, LLC

Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...

The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...

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

Class II — Potential Health HazardOngoing
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: WESTCREEK H&R SELF RISE AP FLR 25LB and 50LB Recalled by Ardent Mills, LLC...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: MEMBERS MARK SELF RISE FLR 25LB Recalled by Ardent Mills, LLC Due to...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund