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. 2,519 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,519 in last 12 months

Showing 1118111200 of 47,764 recalls

Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2022· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed dissolution...

The Issue: Failed dissolution specifications: OOS for dissolution at the 12-month...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 7, 2022· Olympus Corporation of the Americas

Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...

The Issue: Mis-wired component-the improperly wired component can result in additional...

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Insulin Glargine (Insulin glargine-yfgn) Injection Recalled by Mylan...

The Issue: Labeling: Missing label: Label missing from some prefilled pens.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2022· TOVALA

Recalled Item: Tovala Gochujang-Glazed Pork Chop Bowl meal No.9-A Recalled by TOVALA Due to...

The Issue: Product contains undeclared peanut

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2022· TOVALA

Recalled Item: Tovala Gochujang-Glazed Salmon Bowl meal No.18-A Recalled by TOVALA Due to...

The Issue: Product contains undeclared peanut

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2022· Zap Surgical Systems

Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to Software...

The Issue: Software issue identified in cases of initial patient setup with large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 0.5ml Code: OT005 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD Recalled...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 2.5ml Code: OT25 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05 Recalled by Medicina...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 5ml Code: OTH05 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 1ml Code: OT01 Recalled by Medicina Uk Ltd Due to...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 2.5ml Code: OTH25 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 1ml Code: OTH01 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

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

Class II — Potential Health HazardOngoing
FoodJuly 3, 2022· ARBORYPHARM FOODS INC.

Recalled Item: Natreve Vegan Protein Powder 10 servings Recalled by ARBORYPHARM FOODS INC....

The Issue: Undeclared allergen; milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 1, 2022· Intuitive Surgical, Inc.

Recalled Item: Da Vinci S/Si Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Due to the potential for unexpected motion caused by the partial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2022· Intuitive Surgical, Inc.

Recalled Item: Da Vinci X/Xi Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Due to the potential for unexpected motion caused by the partial...

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

Class II — Potential Health HazardOngoing
DrugJune 30, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Succinylcholine Chloride Injection Recalled by Nephron Sterile Compounding...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund