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. 2,404 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,404 in last 12 months

Showing 2124121260 of 48,219 recalls

Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Preformed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Controls Ptoduct Usage: The ARCHITECT BNP Controls are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) Uncuffed 6.0 mm Recalled by Teleflex Medical Due to...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT: 1) Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan: 1) HVT 6.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to This...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS Recalled by Teleflex Medical Due to This voluntary...

The Issue: This voluntary recall is due to reported complaints (<0.0025% of all in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Cook Inc.

Recalled Item: Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm Recalled by...

The Issue: Multiple complaints were received for balloons bursting below the rated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2019· Abbott Laboratories

Recalled Item: ARCHITECT BNP Calibrators Ptoduct Usage: The ARCHITECT BNP Calibrators are...

The Issue: Presence of a time dependent, stability drift in patient and control results...

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

Class III — Low RiskOngoing
FoodMay 24, 2019· LAIRD SUPERFOOD INC

Recalled Item: Performance Mushrooms product is dried mushroom blend of 4 different...

The Issue: The product is incorrectly labeled with 14 mg of Iron and 78% DV when the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 23, 2019· Richard Wolf Medical Instruments Corp.

Recalled Item: E-Line Cutting Electrode 11.5Fr Mono 0 degrees Recalled by Richard Wolf...

The Issue: E-Line Cutting Electrode package 8416.0305 contains E-Line Hook Electrode...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2019· Anewmed Corporation

Recalled Item: Various products which were contract sterilized. Recalled by Anewmed...

The Issue: The contract sterilizer did not have adequate packaging data to support the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2019· Obalon Therapeutics Inc

Recalled Item: Obalon Balloon System with Model 4300 Touch Dispenser Touchscreen Recalled...

The Issue: During initial set-up and/or replacement of the dispenser batteries, the...

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

Class II — Potential Health HazardOngoing
DrugMay 23, 2019· Pharm D Solutions, LLC

Recalled Item: Ipamorelin Acetate 9 mg/9mL Injectable vials Recalled by Pharm D Solutions,...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Complaint received of metal piece identified in the product bottle prior to...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2019· Pharm D Solutions, LLC

Recalled Item: Testosterone 200 mg/mL Recalled by Pharm D Solutions, LLC Due to Lack of...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2019· Pharm D Solutions, LLC

Recalled Item: Sermorelin/GHRP-2 9 mg/6 mg vials Recalled by Pharm D Solutions, LLC Due to...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund