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. 2,535 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,535 in last 12 months

Showing 78217840 of 48,219 recalls

Medical DeviceAugust 5, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides Recalled by Ortho-Clinical...

The Issue: Samples containing high levels of ALKP (or an interfering substance) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: HUDSON RCI Addipak Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Product dispositioned for scrap for sterility failure investigation that was...

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

Class I — Serious Health HazardOngoing
DrugAugust 3, 2023· APG SEVEN, INC

Recalled Item: Vegetal Vigra Recalled by APG SEVEN, INC Due to Marketed Without an Approved...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 3, 2023· Ansell Healthcare Products LLC

Recalled Item: NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell...

The Issue: Some surgical glove sterile pouches were not completely sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· LivaNova Deutschland GmbH

Recalled Item: 3T Heater Cooler System Recalled by LivaNova Deutschland GmbH Due to The...

The Issue: The firm's labeling (Quick Guide) contains incorrect information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· Ansell Healthcare Products LLC

Recalled Item: GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell Healthcare...

The Issue: Some surgical glove sterile pouches were not completely sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· Accuray Incorporated

Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...

The Issue: It is possible the upper roller bracket in the Radixact System gantry...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2023· Aurobindo Pharma USA Inc.

Recalled Item: Rasagiline Tablets 0.5mg Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed dissolution specifications - results obtained were below spec average.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Helix Pain Relieving Cream (Menthol 7.4%) Recalled by Parker Laboratories,...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Helix Tri-Active Therapy Cream (Camphor 3.2% Recalled by Parker...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Helix CBD Therapy Cream (Menthol 7.4%) Recalled by Parker Laboratories, Inc....

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Helix CBD Clinical Cream (Menthol 7.4%) Recalled by Parker Laboratories,...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2023· Parker Laboratories, Inc.

Recalled Item: Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%) Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 2, 2023· Philips Healthcare

Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...

The Issue: Philips has identified three software issues with compliance concerns to...

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

Class II — Potential Health HazardOngoing
FoodAugust 1, 2023· Lipari Foods Operating Company, LLC.

Recalled Item: IO Inspired Organics brand Organic Raw Walnut Halves & Pieces Recalled by...

The Issue: undeclared walnuts in ingredient and contains statement

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 1, 2023· Skytron, LLC

Recalled Item: GS70H Salus Surgical Table Recalled by Skytron, LLC Due to When the control...

The Issue: When the control of the operating table was used in Bluetooth mode, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2023· Skytron, LLC

Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...

The Issue: When the control of the operating table was used in Bluetooth mode, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2023· Medtronic Sofamor Danek USA Inc

Recalled Item: Magnifuse Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The incorrect product labeling was applied to the product indicating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP) Recalled by Datascope...

The Issue: Users were reporting that the device was not charging as expected. It was...

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

Class I — Serious Health HazardOngoing