Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,431 recalls have been distributed to Oklahoma in the last 12 months.
Showing 40181–40200 of 49,976 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010...
The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number:...
The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.