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. 1,677 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,677 in last 12 months

Showing 4656146580 of 48,219 recalls

FoodAugust 31, 2012· Ready Pac Foods Inc

Recalled Item: Starbucks¿ Seasonal Harvest Fruit Blend Recalled by Ready Pac Foods Inc Due...

The Issue: Firm is voluntarily recalling, out of an abundance of caution, packaged...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 31, 2012· Ready Pac Foods Inc

Recalled Item: Ready Pac¿ Seasons Choice" Recalled by Ready Pac Foods Inc Due to Potential...

The Issue: Firm is voluntarily recalling, out of an abundance of caution, packaged...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 31, 2012· Ready Pac Foods Inc

Recalled Item: Ready Pac¿ Sliced Mango Recalled by Ready Pac Foods Inc Due to Potential...

The Issue: Firm is voluntarily recalling, out of an abundance of caution, packaged...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 31, 2012· Ready Pac Foods Inc

Recalled Item: Ready Pac¿ Sweet Sunshine Platter Recalled by Ready Pac Foods Inc Due to...

The Issue: Firm is voluntarily recalling, out of an abundance of caution, packaged...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 31, 2012· Ready Pac Foods Inc

Recalled Item: Fruit Mixes: 1) Dining In¿ Super Fruit Medley Recalled by Ready Pac Foods...

The Issue: Firm is voluntarily recalling, out of an abundance of caution, packaged...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 31, 2012· Ready Pac Foods Inc

Recalled Item: Mango: 1) Dining In¿ Mango Recalled by Ready Pac Foods Inc Due to Potential...

The Issue: Firm is voluntarily recalling, out of an abundance of caution, packaged...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 31, 2012· Ready Pac Foods Inc

Recalled Item: Walmart¿ Seasonal Blend Recalled by Ready Pac Foods Inc Due to Potential...

The Issue: Firm is voluntarily recalling, out of an abundance of caution, packaged...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 30, 2012· Vascular Solutions, Inc.

Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...

The Issue: Vascular Solutions, Inc., became aware of a potential problem involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2012· Medtronic Sofamor Danek USA Inc

Recalled Item: ATLANTIS(R) Anterior Cervical Plate System VARIABLE ANGLE SCREW MODULE...

The Issue: Lines on the screw gauge may not placed on the caddy properly which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2012· Medtronic Sofamor Danek USA Inc

Recalled Item: ATLANTIS(R) Anterior Cervical Plate System FIXED ANGLE SCREW MODULE Recalled...

The Issue: Lines on the screw gauge may not placed on the caddy properly which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2012· Medtronic Sofamor Danek USA Inc

Recalled Item: PREMIER(R) Anterior Cervical Plate System SCREW BLOCK Recalled by Medtronic...

The Issue: Lines on the screw gauge may not placed on the caddy properly which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2012· Hospira Inc.

Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...

The Issue: The Symbiq pump touchscreen may not respond to user selection, may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2012· Remington Medical Inc.

Recalled Item: Automatic Cutting Needles Recalled by Remington Medical Inc. Due to...

The Issue: Sterility of the product may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2012· Hospira Inc.

Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...

The Issue: The Symbiq pump touchscreen may not respond to user selection, may...

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

Class I — Serious Health HazardOngoing
DrugAugust 29, 2012· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: A single visible particulate was observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2012· Bristol-myers Squibb Company

Recalled Item: BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only Recalled by...

The Issue: Superpotent (Single Ingredient) Drug: All BiCNU lots within expiration which...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 28, 2012· Hospira Inc.

Recalled Item: Preservative-Free MORPHINE Sulfate Injection Recalled by Hospira Inc. Due to...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2012· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2012· James G. Cole, Inc.

Recalled Item: I-C Drops Recalled by James G. Cole, Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The product is being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 28, 2012· SpineFrontier, Inc.

Recalled Item: Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors...

The Issue: Inspan Compressors may break at weld causing a loss of compression

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

Class II — Potential Health HazardOngoing