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 17221–17240 of 47,764 recalls
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...
The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...
The Issue: The plastic housing on the device may fracture
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daptomycin for Injection Recalled by Mylan Institutional LLC Due to Presence...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Medica Acne System Recalled by Allergan PLC Due to SUBPOTENT DRUG:...
The Issue: SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Medica Acne Treatment Lotion (Benzoyl Peroxide 2.5%) Recalled by...
The Issue: SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Cross contamination with other products - OOS discovered during routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 40 (102cm) Appx 4.4ml Ext Set 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: 149 IN (378cm) APPX 19.1 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: Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98 IN (249cm) APPX 8.4 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: 20 cm (8 IN) APPX 1.0ml 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: 112 IN (284cm) APPX 14.7ml 15 DROP SET 2 MicroClave Recalled by ICU Medical,...
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: 109" (277 cm) Appx 8.6 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: 7" (18 cm) Appx 0.25 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: APPX 0.75 ml Recalled by ICU Medical, Inc. Due to Identification of a...
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" (13 cm) Appx 0.39 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: 7" (18 cm) Appx 0.31 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.