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. 2,512 recalls have been distributed to Hawaii in the last 12 months.
Showing 12641–12660 of 27,645 recalls
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CapsoCAM Plus Recalled by Capso Vision, Inc. Due to Capsule Endoscopy...
The Issue: Capsule Endoscopy System: a defect present in the capsule window may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...
The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...
The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT cTnI cartridge Recalled by Abbott Point Of Care Inc. Due to i-STAT¿...
The Issue: i-STAT¿ cTnI blue cartridges may generate a higher than expected number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.