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. 2,480 recalls have been distributed to Hawaii in the last 12 months.
Showing 14981–15000 of 27,645 recalls
Recalled Item: Ysio (model number 10281013 or 10281163) with Tube stand 3D Recalled by...
The Issue: In rare cases of high clinical workload, the steel cables inside the lifting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multix Fusion system is a radiographic system: Models: Multix Fusion...
The Issue: Steel cables inside the lifting column of the overhead tube, may rapture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...
The Issue: Expiration date on the label is incorrect. Correct expiration date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Gauze Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (10 mL Size) Recalled by Instrumentation Laboratory Co....
The Issue: There is a potential for increased imprecision, out of range quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sterEOS workstation Recalled by EOS Imaging Due to 3D projections may be...
The Issue: 3D projections may be incorrect when the pair of images used is a secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix AMD Antimicrobial Bandage Roll Recalled by COVIDIEN LLC Due to...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module...
The Issue: A software malfunction of the infuser when used with a MedNet Custom Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Air Optix Night & Day Aqua (lotrafilcon A) Recalled by Allied Vision...
The Issue: Potentially counterfeit products in/and counterfeit packaging were imported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOLOGIX AFX/AFX2 Recalled by Endologix Due to Endologix is notifying...
The Issue: Endologix is notifying physicians of patient tailored surveillance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS Recalled by Oridion Medical 1987...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (US) N Recalled by Oridion Medical 1987 Ltd. Due to The...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (COV-INTL) N W/PRINTER ROHS Recalled by Oridion Medical 1987...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (US) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.