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. 2,342 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,342 in last 12 months

Showing 3582135840 of 48,219 recalls

FoodJune 12, 2015· Dairy Farmers OF America Inc

Recalled Item: Imitation Pasteurized Process Cheese Food: SANDWICH MATE 24/6.56OZ IMITATION...

The Issue: Dairy Farmers of America Inc. is recalling a number of cheese products due...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 12, 2015· Dairy Farmers OF America Inc

Recalled Item: Non-Fat Pasteurized Prepared Cheese Product: FOOD CLUB 12/12OZ AMER FAT...

The Issue: Dairy Farmers of America Inc. is recalling a number of cheese products due...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 12, 2015· Dairy Farmers OF America Inc

Recalled Item: Pasteurized Prepared Cheese Product: BORDEN 12/8OZ SWISS SINGLES CHEESE PROD...

The Issue: Dairy Farmers of America Inc. is recalling a number of cheese products due...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2015· CryoLife, Inc.

Recalled Item: On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement...

The Issue: Incorrect product label. The type of Sewing Ring was mislabeled as being a...

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

Class II — Potential Health HazardOngoing
DrugJune 12, 2015· GC Natural Nutrition, Inc.

Recalled Item: PYROLA Advanced Joint Formula capsules Recalled by GC Natural Nutrition,...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 11, 2015· Justright Surgical, LLC

Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...

The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Justright Surgical, LLC

Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...

The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2015· Abbott Laboratories

Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...

The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2015· Synthes (USA) Products LLC

Recalled Item: Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA)...

The Issue: The height of one of the three guiding pins of the Helical Blade Inserter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2015· Northern Digital Inc.

Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...

The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...

The Issue: There is a potential issue that could result to collision between the C-arm...

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

Class II — Potential Health HazardOngoing
DrugJune 10, 2015· AstraZeneca Pharmaceuticals LP

Recalled Item: NEXIUM¿ (esomeprazole magnesium) Recalled by AstraZeneca Pharmaceuticals LP...

The Issue: Presence of Foreign Tablets/Capsules: Confimed customer compliant by a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2015· The Harvard Drug Group, LLC

Recalled Item: OXYCODONE HCl C-II Tablets Recalled by The Harvard Drug Group, LLC Due to...

The Issue: Superpotent Drug: Confirmed customer complaint of a single unit dose blister...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 9, 2015· Alliance Partners LLC

Recalled Item: Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill...

The Issue: Inadequate interference between the screw and the plate when screw implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2015· Omnilife Science Inc.

Recalled Item: Offset Femoral Alignment Guide 4mm x 6¿ Recalled by Omnilife Science Inc....

The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2015· Olympus Scientific Solutions Americas

Recalled Item: Olympus Scientific Solutions Americas Analytical X-ray System. Delta...

The Issue: Higher than published scatter around the probe head when testing some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2015· Omnilife Science Inc.

Recalled Item: Offset Femoral Alignment Guide Recalled by Omnilife Science Inc. Due to The...

The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...

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

Class II — Potential Health HazardOngoing
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: E3 CREAM Recalled by Life Science Pharmacy Inc Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: ESTRIOL Vaginal Creams Recalled by Life Science Pharmacy Inc Due to...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2015· Life Science Pharmacy Inc

Recalled Item: ESTRIOL Face Creams Recalled by Life Science Pharmacy Inc Due to Penicillin...

The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin

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

Class II — Potential Health HazardOngoing
Refund