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. 1,027 recalls have been distributed to Hawaii in the last 12 months.
Showing 17321–17340 of 47,764 recalls
Recalled Item: DISTALE - 203 cm (80") Bifuse Ext Set w/6 Gang 1o2 Manifold Recalled by ICU...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" (15 cm) Appx 0.26 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11 IN (28cm) APPX 1.5ml EXT SET NanoClave Recalled by ICU Medical, Inc. Due...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 IN (25cm) APPX 1.1ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx 0.30 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clave Stopcock. 1 unit per pouch Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 IN(13cm) APPX 0.87ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8" (20 cm) Appx 0.33 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9.5" (24 cm) 0.53 ml Recalled by ICU Medical, Inc. Due to Identification of...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5" (14 cm) Appx 0.50 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 226 cm (89 IN) APPX 2.7ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 78 IN (198cm) APPX 10.0 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 58cm (23 IN) APPX 2.1 ml EXT SET Smallbore PUR Yellow w/6-Port Clave...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60 IN(152cm) APPX 0.85ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5" (19 cm) Appx 0.59 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 99 IN (251cm) APPX 12.6ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYNEX Agility Recalled by Dynex Technologies, Inc. Due to Control samples...
The Issue: Control samples aspirated from wrong SmartKit on the Agility. Agility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by Granules...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone/Anastrozole Pellet 100/6 mg Recalled by MasterPharm LLC Due to...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.