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. 2,330 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,330 in last 12 months

Showing 3968139700 of 48,219 recalls

DrugAugust 27, 2014· Qualitest Pharmaceuticals

Recalled Item: OXYCODONE and ACETAMINOPHEN Recalled by Qualitest Pharmaceuticals Due to...

The Issue: Failed Tablet/Capsule Specifications: Broken tablets found in sealed bottles.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2014· Sage Products Inc

Recalled Item: Comfort Shield Barrier Cream Cloths with dimethicone a) 8 count NDC...

The Issue: Microbial Contamination of Non-Sterile Products: Comfort Shield Barrier...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 27, 2014· Mondelez Global Llc

Recalled Item: Chiclets Gum Recalled by Mondelez Global Llc Due to Undeclared Soy

The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 27, 2014· Mondelez Global Llc

Recalled Item: 1) Chiclets Peppermint Gum Recalled by Mondelez Global Llc Due to Undeclared Soy

The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 27, 2014· Mondelez Global Llc

Recalled Item: Chiclets Assorted Variety Multipak - Fruit Flavor Gum Recalled by Mondelez...

The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 27, 2014· Mondelez Global Llc

Recalled Item: Chiclets Gum Recalled by Mondelez Global Llc Due to Undeclared Soy

The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 27, 2014· Mondelez Global Llc

Recalled Item: 1) Chiclets Fruit Flavor Gum Recalled by Mondelez Global Llc Due to...

The Issue: Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 27, 2014· DePuy Orthopaedics, Inc.

Recalled Item: Charnley PN Retract & Handle Recalled by DePuy Orthopaedics, Inc. Due to The...

The Issue: The small extraction peg of the Charnley Pin Retractor and Handle set is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2014· Mckesson Information Solutions LLC

Recalled Item: McKesson Cardiology" Hemo intended for complete physiological/hemodynamic...

The Issue: Software Error: The McKesson Cardiology Hemo calculation section incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: The Ysio Systems with software version VC10 The Ysio enables Recalled by...

The Issue: Siemens discovered that an unlikely error may occur on the Ysio system with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Medical Patient Monitor is a Physiological Recalled by Spacelabs...

The Issue: The clinician did not realize the monitor was in END CASE mode and was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m)...

The Issue: Sterility of device is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes Part number: 8900-4012...

The Issue: Sterility of device is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bard Peripheral Vascular Inc

Recalled Item: Bard DuaLok Breast Lesion Localization Wire Recalled by Bard Peripheral...

The Issue: Bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes ((singles) Part...

The Issue: Sterility of device is not assured

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

Class II — Potential Health HazardOngoing
DrugAugust 25, 2014· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsule Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2014· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsule Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit Recalled by...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing