Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 989 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
989 in last 12 months

Showing 21121–21140 of 48,376 recalls

Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 19FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 19FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 15FR Cardinal PN:JP-2223 An...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 19FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Smith & Nephew Negative Pressure Wound Therapy 15FR Channel Wound Recalled...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Sentinel CH SpA

Recalled Item: MULTIGENT Lithium-intended for the quantitation of lithium in serum or...

The Issue: Added an additional SmartWash parameter for the Lithium and Alinity c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2019· Degania Silicone, Ltd.

Recalled Item: Cardinal Health Jackson-Pratt Channel Drain 15FR Recalled by Degania...

The Issue: 15FR and 19FR round fluted drain channel drain may break during use (mostly...

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

Class II — Potential Health HazardOngoing
DrugJune 28, 2019· Fresenius Kabi USA, LLC

Recalled Item: Fluorouracil Injection Recalled by Fresenius Kabi USA, LLC Due to Presence...

The Issue: Presence of Particulate Matter; glass particulates

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: MiniMed Paradigm 512 Insulin pump Recalled by Medtronic MiniMed Due to The...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: N Cuvette Segments for BN ProSpec System-IVD a system for Recalled by...

The Issue: Iincreased (falsely elevated) Albumin results compared to expected results

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: MiniMed Insulin Pump Recalled by Medtronic MiniMed Due to The action is...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Agfa N.V.

Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Recalled by Agfa...

The Issue: The exposed area of fluo exams possibly does not match the active area of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing