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. 2,540 recalls have been distributed to Hawaii in the last 12 months.
Showing 9301–9320 of 47,764 recalls
Recalled Item: Norepinephrine Bitartrate Injection Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Impurities/Degradation Specifications: Above the specification limits...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dodex Injectable Cyanocobalamin Injection Recalled by Accord Healthcare,...
The Issue: Sub-potent drug: assay test result below specifications at 9-month timepoint.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs Recalled by...
The Issue: The case and each (i.e. packet) labels for the DYND3000xxP series do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isopropyl Alcohol Antiseptic 75% Recalled by Jarman's Midwest Cleaning...
The Issue: CGMP deficiencies: Product manufactured at the same site where FDA testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SOFT HANDS Alcohol Antiseptic 80% Recalled by Jarman's Midwest Cleaning...
The Issue: Chemical Contamination: FDA testing found Presence of methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alcohol Antiseptic 80% Recalled by Jarman's Midwest Cleaning Systems, Inc....
The Issue: Chemical Contamination: FDA testing found Presence of methanol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bevacizumab 2.5 mg/0.1 mL Recalled by Pine Pharmaceuticals, LLC Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Lot code on primary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Montelukast Sodium Oral Granules USP Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications: failed impurities for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tab Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...
The Issue: CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tab Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...
The Issue: CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tab Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...
The Issue: CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Immundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended...
The Issue: Marketed without a 510k
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TDHisto/Cyto - A software product used for managing medical information...
The Issue: In a specific use case, when printing labels for slides, some labels may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM NEUROTUBE Recalled by Baxter Healthcare Corporation Due to The product...
The Issue: The product is brittle and potentially crumbling upon handling or when being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM Recalled by Smith &...
The Issue: A mispack occurred during the manufacturing process, resulting in the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. BIOPSY FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 6.6FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Recalled by...
The Issue: A manufacturing error, resulted in a less than specified diameter of adult...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.