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. 2,375 recalls have been distributed to Hawaii in the last 12 months.
Showing 25081–25100 of 27,645 recalls
Recalled Item: AperFix AM Femoral Implant Recalled by Cayenne Medical Inc. Due to Potential...
The Issue: Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempa DOT Single-Use Clinical Thermometer Medical Indicators Made in U.S.A....
The Issue: TempaDot products may have been mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe...
The Issue: Visible orange/ brown particulate on the needles of the 29g Hypodermic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acuson SC2000 volume imaging ultrasound systems at software version 3.0....
The Issue: Software issue results in inaccurate 3D image may result in ablation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tray Surgical Recalled by Medtronic Xomed, Inc. Due to The firm will recall...
The Issue: The firm will recall and replace the identified instrument trays in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiohead Access Point 1.4 GHz Radiohead Access Point Firmware versions:...
The Issue: IntelliVue Smart-hopping 1.4 GHz Access Point may experience unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 1) Asnis III Cannulated Screw 4.0x40mm TL Recalled by Stryker...
The Issue: Stryker received a report that the length of the cannulated screw asnis III,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain AG. For use in the screening and detection of cervical cancer....
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Tecan US-II. For use in the screening and detection Recalled by...
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mullins Transseptal Adult 7F Recalled by Medtronic Inc. Cardiac...
The Issue: Medtronic identified a specific labeling issue for specific lots of Mullins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PrepStain Tecan US-I. For use in the screening and detection Recalled by...
The Issue: PrepStain system rack setting was incorrectly entered on one PrepStain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Suction Wand Model S099B Recalled by Sorin Group USA,...
The Issue: Sorin Group is recalling certain lots of Edwards Lifesciences Suction Wand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The patient support may move in an unintended manner if the footswitch cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pCO2 D788 Membranes. Distributed by Radiometer America Recalled by...
The Issue: RADIOMETER has become aware that some D788 pCO2 membranes can cause biased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Reservoirs Recalled by Medtronic MiniMed Due to...
The Issue: Medtronic is recalling certain lots of Medtronic MiniMed Paradigm Reservoirs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Triathlon tibial alignment ankle clamp...
The Issue: Cracks or fracture of the Triathlon Tibial Alignment Ankle Clamp, an instrument.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.