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. 2,475 recalls have been distributed to Hawaii in the last 12 months.
Showing 16081–16100 of 47,764 recalls
Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxyzine Hydrochloride Oral Solution Recalled by Morton Grove...
The Issue: Failed Impurities/Degradation Specification: OOS for the following - unknown...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vumerity (diroximel fumarate) delayed-release capsule Recalled by Biogen MA...
The Issue: Failed dissolution specifications: out-of-specification test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine for Injection 100 mg/vial Recalled by Shilpa Medicare Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 100 mg Recalled by Shilpa Medicare Limited Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 400 mg Recalled by Shilpa Medicare Limited Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Busulfan Injection 60 mg/10 mL (6 mg/mL) Recalled by Shilpa Medicare Limited...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docetaxel Injection USP 160 mg/8mL (20 mg/mL) Recalled by Shilpa Medicare...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas 8000 modular analyzer series (i.e. Recalled by Roche Diagnostics...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-110: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas pro integrated solutions (cobas pro ISE Recalled by Roche...
The Issue: Potential for Changed Configuration Settings on the cobas 8000 modular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-105: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix" PMIC-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.