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 2234122360 of 48,219 recalls

Medical DeviceFebruary 11, 2019· Smiths Medical ASD Inc.

Recalled Item: Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device...

The Issue: Incorrect needle length and gage.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2019· Fenwal Inc

Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...

The Issue: The optional Vacuum Unit may stop working and display the failure message...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2019· McDaniel Life-Line LLC

Recalled Item: Indian Herb Paste (a dietary supplement) Ingredients: Galangal Recalled by...

The Issue: Unapproved new drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 8, 2019· McDaniel Life-Line LLC

Recalled Item: Life-Line tm Catalytic Activated Energy Water Recalled by McDaniel Life-Line...

The Issue: Unapproved new drug

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 8, 2019· World Waters, LLC dba WTRMLN WTR

Recalled Item: Watermelon Recalled by World Waters, LLC dba WTRMLN WTR Due to Cold Pressed...

The Issue: Cold Pressed Juice Watermelon WTRMLN WTR Original 12 packs due to the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2019· Canon Medical System, USA, INC.

Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...

The Issue: Table tilts without operator involvement as a result of liquid spilling into...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...

The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 8, 2019· Draegar Medical Systems, Inc.

Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...

The Issue: The firm is recalling their Delta family of patient monitors software due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Draegar Medical Systems, Inc.

Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...

The Issue: The firm is recalling their Delta family of patient monitors software due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...

The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...

The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.

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

Class II — Potential Health HazardOngoing
DrugFebruary 7, 2019· ACP Nimble Buyer, Inc.

Recalled Item: Mometasone Furoate Cream Recalled by ACP Nimble Buyer, Inc. Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 7, 2019· Cordis Corporation

Recalled Item: Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled...

The Issue: Frayed pieces of the mounting card being inside the primary packaging.

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

Class III — Low RiskOngoing
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Express Gel Hand Sanitizer (Ethyl Alcohol 70%) Recalled by Ecolab Inc Due to...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Moisturizing Gel Hand Sanitizer (Ethyl Alcohol 62%) Recalled by Ecolab Inc...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Advanced Gel Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc Due...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%) Recalled by Ecolab Inc...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Ecolab Inc

Recalled Item: Gel Hand Sanitizer (Ethyl Alcohol 70%) Recalled by Ecolab Inc Due to...

The Issue: Chemical Contamination: low levels of various substituted benzene (aromatic)...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 20 Units added to NS 1000 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 30 Units added to NS 500 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund