Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,411 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,411 in last 12 months

Showing 3974139760 of 49,744 recalls

Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUX Material Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUX Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)IR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Leonhard Lang Gmbh

Recalled Item: GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing...

The Issue: The firm discovered that during the use of these defibrillation electrodes a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 3, 2014· Iris Diagnostics

Recalled Item: RTH8 Rotor Recalled by Iris Diagnostics Due to Iris International is...

The Issue: Iris International is recalling the RTH8 Rotor used in the StatSpin Express...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Teleflex Medical

Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...

The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2014· ReNew Life Formulas, Inc.

Recalled Item: PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs...

The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2014· ReNew Life Formulas, Inc.

Recalled Item: PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle Recalled by...

The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerator: ARTISTE Recalled by Siemens Medical Solutions...

The Issue: Use of any unauthorized third-party components on Siemens LINACs may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult AirLife dual-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife single-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife Dual- Recalled by Vyaire Medical Due to Manufacturing error...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing