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 26361–26380 of 27,645 recalls
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B...
The Issue: Ortho Clinical Diagnostics is recalling certain lots of the Vitros Anti-HBs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADstream software. Product Usage: CADstream is an image processing system...
The Issue: An incorrect biopsy or missed target could result if the incorrect grid is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical Advincula Arch Recalled by Cooper Surgical, Inc. Due to...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...
The Issue: This notice is being provided in follow up to the field correction initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posey Biothane Restraint Cuffs Recalled by J T Posey Company Due to The firm...
The Issue: The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical RUMI Arch Recalled by Cooper Surgical, Inc. Due to Excessive...
The Issue: Excessive pressure exerted on the uterine tip when attached to the Arch may,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Overhead Rail System Recalled by Hill-Rom, Inc. Due to Liko/Hill-Rom to...
The Issue: Liko/Hill-Rom to date has received two reports from facilities alleging that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraosseous Fixation System (IFS) 1.7 mm Recalled by Orthohelix Surgical...
The Issue: The firm was notified by a customer that there was a burr on the inside end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Stationary radiographic system Recalled by Philips...
The Issue: When the operator for a wall stand view selects an "image rotation"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost Software Version R2.0.2 Product Usage: This system...
The Issue: With Digital Diagnost R2.0.2 a mirrored "R in a circle" is burnt into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Recalled by Cordis Corporation Due to Affected lots of Cordis ExoSeal...
The Issue: Affected lots of Cordis ExoSeal (TM) VCD have been sterilized using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Single Channel Infusion Pumps with Plug-and-Play Modules that...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiples Anspach Micro Curved Attachments (MCA) and Curved Burr Support...
The Issue: During a recent review of documentation Anspach determined that the current...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Single Channel Infusion Pumps with Hospira Mednet Software Recalled...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiOM Rechargeable Li Ion 22.2 V Battery and BiOM Lithium Recalled by iwalk...
The Issue: Battery may over-heat during charging and smoke
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Single Channel Infusion Pumps with Hospira MedNet...
The Issue: The volume control knob on some Plum A+ single channel infusers (located on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer Recalled by Beckman...
The Issue: Beckman Coulter is recalling the AU8500 Clinical Chemistry Analyzer because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...
The Issue: A manufacturing defect has been identified which could results in the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...
The Issue: A manufacturing defect has been identified which could results in the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.