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. 2,412 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,412 in last 12 months

Showing 2082120840 of 47,764 recalls

DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Naloxone HCL Preserved INJ Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Droperidol Injectable Sterile Solution Recalled by Premier Pharmacy Labs Inc...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Brilliant Blue Ophthalmic PF INJ Recalled by Premier Pharmacy Labs Inc Due...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Atropine Sulfate PF INJ Recalled by Premier Pharmacy Labs Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: ChlorproMAZINE HCL INJ Recalled by Premier Pharmacy Labs Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Neostigmine Methylsulfate Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Lidocaine 0.5%/Phenylephrine 0.75% P.F. INJ Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 18, 2019· Mott's LLP

Recalled Item: Penafiel Mineral Spring Water 600mL (20.3 FL OZ) and Penafiel Recalled by...

The Issue: Elevated levels of inorganic arsenic

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed appropriately, the battery may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...

The Issue: If battery maintenance is not performed appropriately, the battery may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...

The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: Battery short-run times and unanticipated stoppage may be due to user not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2019· Datascope Corp.

Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...

The Issue: If battery maintenance is not performed per instructions, the battery may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugJune 17, 2019· Bausch & Lomb

Recalled Item: Lotemax (loteprednol etabonate ophthalmic gel 0.5%) Recalled by Bausch &...

The Issue: Failed Stability Specifications: Out of specification for viscosity.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci Surgical System Recalled by Intuitive Surgical, Inc. Due to One da...

The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 14, 2019· Golden State Medical Supply Inc.

Recalled Item: Losartan Potassium Recalled by Golden State Medical Supply Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund