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. 2,293 recalls have been distributed to Hawaii in the last 12 months.
Showing 42821–42840 of 47,764 recalls
Recalled Item: STERILE SAMPLE CATH LAB PACK Recalled by Medline Industries, Inc. Due to...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH ANGIOGRAPHY DRAPE PACK Recalled by Medline Industries, Inc. Due to...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIO PACK #2 Recalled by Medline Industries, Inc. Due to Guidewire .035x150...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIOGRAPHY PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH LAB CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Fabius GS Premium Recalled by Draeger Medical, Inc. Due to During...
The Issue: During final testing of the Draeger Fabius GS Premium, Fabius OS, and Fabius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARBOplatin Injection Recalled by Teva Pharmaceuticals USA, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: The required reduction of endotoxin was not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens EasyLink Informatics System V4.0/V5 Siemens Recalled by Siemens...
The Issue: May not perform as intended under certain conditions, causing the release of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument Sternal Zip Flex System intended for use...
The Issue: When using the 1st generation Zip Fix Application Instrument it is possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (1 unit) Recalled by Codman & Shurtleff, Inc. Due to Drug flow...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (6 units) Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cypher MIS Screw System Recalled by Ebi, Llc Due to Several complaints were...
The Issue: Several complaints were reported to exhibit screw head splay in the Cypher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J.R. Jack Rabbit All Natural Herbal Supplement Recalled by Jack Rabbit, Inc...
The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.