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 1112111140 of 47,764 recalls

Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN):RLPC-35-180 ORDER...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RPC-35-180 Recalled...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWS-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN)RFPC-35-180 ORDER...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPW-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-150...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-18-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Cook Incorporated

Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-80...

The Issue: Product did not meet the acceptance criteria for packaging testing, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 7600 Integrated System with Version 3.7.2 and below Recalled by...

The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS XT 3400 Chemistry System with Version 3.7.2 and below Recalled by...

The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...

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

Class II — Potential Health HazardOngoing
DrugJuly 18, 2022· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Irbesartan Tablets Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2022· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Irbesartan Tablets Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due to...

The Issue: Failed dissolution specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 18, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Recalled by...

The Issue: Negative bias with patient samples. The mean patient sample bias range from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2022· Becton Dickinson & Company

Recalled Item: BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System...

The Issue: Incorrect expiration date listed on the product labels. The expiration date...

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

Class II — Potential Health HazardOngoing
DrugJuly 15, 2022· Vi-Jon, LLC

Recalled Item: Walgreens Recalled by Vi-Jon, LLC Due to Microbial contamination of...

The Issue: Microbial contamination of non-sterile products.

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 15, 2022· Vi-Jon, LLC

Recalled Item: Kroger Recalled by Vi-Jon, LLC Due to Microbial contamination of non-sterile...

The Issue: Microbial contamination of non-sterile products.

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 15, 2022· Vi-Jon, LLC

Recalled Item: P Recalled by Vi-Jon, LLC Due to Microbial contamination of non-sterile...

The Issue: Microbial contamination of non-sterile products.

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

Class I — Serious Health HazardOngoing
Refund