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. 2,322 recalls have been distributed to Hawaii in the last 12 months.
Showing 40581–40600 of 47,764 recalls
Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...
The Issue: Test Strips may report an inaccurately low INR result. Several patients had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Super ARTHGOLD 500mg Recalled by Sung Soo Kim Due to Undeclared Indomethacin
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Children's Triacting Night Time Cold & Cough with PE (diphenhydramine...
The Issue: Presence of Precipitate: Small amounts of diphenydramine and mannitol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...
The Issue: When using a specific plan update workflow in combination with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...
The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALOPERIDOL DECANOATE INJECTION Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: Presence of Foreign Substance; some bottles may contain debris that was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Phenylephrine component is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxandrolone Tablets Recalled by Upsher Smith Laboratories, Inc. Due to...
The Issue: Labeling: Missing Label; Three cases of product (total of 36 bottles) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80%...
The Issue: Undeclared milk allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...
The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...
The Issue: A stock check revealed broken glass fibers between the connector and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...
The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...
The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.