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. 2,484 recalls have been distributed to Hawaii in the last 12 months.
Showing 13961–13980 of 47,764 recalls
Recalled Item: ELI Recalled by Welch Allyn Inc Mortara Due to The devices malfunction under...
The Issue: The devices malfunction under specific operator workflows.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030H Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0025A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0030 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0020A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0025B Recalled by W L Gore & Associates, Inc. Due...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0030B Recalled by W L Gore & Associates, Inc. Due...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0020 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0025 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA Versions: 4.7 Recalled by BioMerieux SA Due to Under certain...
The Issue: Under certain conditions, there is a risk for a false negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Recalled by...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit (Emergency Use Authorization Recalled by...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force with software syngo.CT VB20 Model #10742326 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.