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. 2,378 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,378 in last 12 months

Showing 2522125240 of 27,462 recalls

Medical DeviceMay 24, 2013· International Biomedical, Ltd.

Recalled Item: VIA Medical Collection Bag Recalled by International Biomedical, Ltd. Due to...

The Issue: International Biomedical has received reports of interference between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Service Replacement 0-Ring. Used in as a service part Recalled by...

The Issue: Incorrect rubber nitrile O-rings distributed instead of the correct material...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is Recalled...

The Issue: The outer sleeve would not fit over the S-LIFT Inserter assembly because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Gyrus Acmi, Incorporated

Recalled Item: GYRUS ACMI Recalled by Gyrus Acmi, Incorporated Due to lack of sterility...

The Issue: lack of sterility assurance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Fenwal Inc

Recalled Item: AMICUS Exchange Kit Recalled by Fenwal Inc Due to Fenwal has initiated a...

The Issue: Fenwal has initiated a voluntary Urgent Product Recall for lot FA12C07070 of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Medium) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Pinook-Usa

Recalled Item: Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen...

The Issue: Failure to submit a premarket submission and gain approval of a medical device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Pinook-Usa

Recalled Item: Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen...

The Issue: Failure to submit a premarket submission and gain approval of a medical device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-820-000S3 T4 Toga w/Inside Shoulder Ties Recalled...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-850-000S2 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-710-000 T4 Pullover Toga (S/M) Sterile Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments0400-750-000 T4 Toga Recalled by Stryker Instruments Div....

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-830-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-850-100 T5 zipper Toga with Peel Away Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-820-100 T5 Zipper Toga with Peel Away Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-850-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-820-000S7 T4 XXL Toga w/T3 Cut Recalled by Stryker...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-720-000S5 T5 Pullover Toga w/Peel Away Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-840-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments0400-720-000 T4 Pullover Toga (L/XL) Sterile Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing