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. 2,549 recalls have been distributed to Hawaii in the last 12 months.
Showing 6321–6340 of 47,764 recalls
Recalled Item: Nimbus II Infusion System Recalled by InfuTronix LLC Due to InfuTronix is...
The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Situate Laparotomy Sponge Recalled by Covidien Due to Packs including 5...
The Issue: Packs including 5 laparotomy sponges may contain incorrect product with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicardipine Hydrochloride Injection Recalled by Eugia US LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicardipine Hydrochloride Injection (2.5mg/mL) Recalled by Eugia US LLC Due...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Phosphate Recalled by Contract Pharmaceuticals Limited Canada...
The Issue: Defective Container: Out of specification for weight due to a slow leakage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Contract...
The Issue: Defective Container: Out of specification for weight due to a slow leakage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin 5mg/ml Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCL 1% (10mg/mL) Recalled by Denver Solutions, LLC DBA Leiters...
The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin PF Recalled by Denver Solutions, LLC DBA Leiters Health Due to...
The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALYARD SURGICAL HOOD Recalled by O&M HALYARD, INC. Due to Mislabeling
The Issue: Product was mislabeled as a Surgical Cap at its dispenser level.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kits that include High Crack Check Valve PN...
The Issue: Pressure relief valve included in certain lots of cardiovascular procedure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Tube Securement Device Recalled by 3M Company - Health Care Business Due...
The Issue: Manufacturing nonconformities are in some lots of the Tube Securement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific iSLEEVE EXPANDABLE Introducer Set Recalled by Boston...
The Issue: Boston Scientific is conducting a removal of specific batches of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROBLEND E3 Foaming Hand Sanitizer Recalled by Seatex LLC Due to CGMP...
The Issue: CGMP Deviations: deficiencies were identified during an FDA inspection of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROBLEND Hand Sanitizer Recalled by Seatex LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: deficiencies were identified during an FDA inspection of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.