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. 2,278 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,278 in last 12 months

Showing 4800148020 of 48,219 recalls

Medical DeviceMay 2, 2011· BRAEMAR, INC.

Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-00...

The Issue: Braemar Inc., became aware of a battery related incident that occurred with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2011· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Recalled by...

The Issue: In Online Entry (OEx) there are two scenarios where a Test result from one...

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

Class III — Low RiskOngoing
FoodApril 14, 2011· The TJX Companies, Inc.

Recalled Item: Mrs. Bridges Scottish Raspberry Preserve ("Jam") Recalled by The TJX...

The Issue: The firm is initiating the recall for Scottish Raspberry Preserve due to...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 13, 2011· Extremity Medical LLC

Recalled Item: IO Fix IntraOsseous Fixation System Recalled by Extremity Medical LLC Due to...

The Issue: Product Event Reports revealed that lag screw passes through washer (e.g....

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

Class II — Potential Health HazardOngoing
DrugApril 6, 2011· Physicians Total Care, Inc.

Recalled Item: Metronidazole Tablets Recalled by Physicians Total Care, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Some tablets had the potential to not...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2011· VistaPharm, Inc.

Recalled Item: Xactdose Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to...

The Issue: Defective container; lidding deformity allows the contained product to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 5, 2011· GE Healthcare, LLC

Recalled Item: GE LightSpeed CT750 HD The GE LightSpeed CT750 HD Computed Recalled by GE...

The Issue: GE Healthcare conducted a recall involving 2 events affecting the GE...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00789502202 VerSys Femoral Head Provisional 22mm +0 00789502203 VerSys...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00789502601 VerSys Femoral Head Provisional 26mm -3.5 00789502602 VerSys...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 12/14 Neck Taper 00789504001 VerSys Femoral Head Provisional 40mm -3.5...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 12/14 Neck Taper 00789503201 VerSys Femoral Head Provisional 32mm -3.5...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2011· Zimmer, Inc.

Recalled Item: 00789503601 VerSys Femoral Head Provisional 36mm -3.5 00789503602 VerSys...

The Issue: Complaints have been received reporting sub-optimal fit between provisional...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2011· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When performing a...

The Issue: When performing a secondary capture generated from GSI Viewer, the header...

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

Class II — Potential Health HazardOngoing