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. 2,367 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,367 in last 12 months

Showing 2964129660 of 48,219 recalls

DrugFebruary 10, 2017· Synergy Rx

Recalled Item: BICARBONATE 10% Recalled by Synergy Rx Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: ADAPALENE 0.1% Recalled by Synergy Rx Due to Lack of Assurance of Sterility:...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: RETINOIC ACID SOLUTION in all strengths including 0.3% Recalled by Synergy...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: TCA PEEL SOLUTION in all strengths including: 5% Recalled by Synergy Rx Due...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Sandoz Inc

Recalled Item: Pioglitazone and Glimepiride Tablets Recalled by Sandoz Inc Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Hospira Inc., A Pfizer Company

Recalled Item: METRONIDazole Injection Recalled by Hospira Inc., A Pfizer Company Due to...

The Issue: Lack of Sterility Assurance: customer report of leaking bag

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2017· Olympus Corporation of the Americas

Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...

The Issue: A damaged temperature sensor at the endoscope's tip can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...

The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Remel Inc

Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...

The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2017· X-Gen Pharmaceuticals Inc.

Recalled Item: Ibuprofen Lysine Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 8, 2017· Amerisource Health Services

Recalled Item: CycloSPORINE Capsules Recalled by Amerisource Health Services Due to Failed...

The Issue: Failed Impurities/Degradations Specifications; out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2017· Del Mar Reynolds Medical, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....

The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...

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

Class II — Potential Health HazardOngoing
DrugFebruary 7, 2017· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2017· Actavis Inc

Recalled Item: Levofloxacin Ophthalmic Solution Recalled by Actavis Inc Due to Failed...

The Issue: Failed Impurities/ Degradation Specifications: OOS for related compound...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF#...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2017· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU)...

The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...

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

Class II — Potential Health HazardOngoing