Product Recalls in Hawaii
Product recalls affecting Hawaii — including food, drugs, consumer products, medical devices, and vehicles distributed to Hawaii. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,338 recalls have been distributed to Hawaii in the last 12 months.
Showing 38221–38240 of 47,764 recalls
Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...
The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...
The Issue: Failed Stability Specifications: Product is subpotent and has out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotoprone Therapy System. The Rotoprone Therapy System is an advanced...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ferno Model 35X PROFlexx Stretchers Recalled by Ferno-Washington Inc Due to...
The Issue: The wheel castor assemblies may be loosening on the stretchers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...
The Issue: Suboptimal routing of the cable may result in increased wear over time....
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: 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.
Recalled Item: Mini Naan Eight (8) nann packaged in coated paper printed Recalled by fgf...
The Issue: The products were shipped without labels declaring the nutrition and...
Recommended Action: Do not consume. Return to store for a refund or discard.