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. 2,566 recalls have been distributed to Hawaii in the last 12 months.

47,764 total recalls
2,566 in last 12 months

Showing 37813800 of 47,764 recalls

Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: SENSE Breast Coil 3.0T 7ch Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 16ch 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Diagnostic Coil 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 7ch 3.0T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: ST SENSE Breast Dx Coil Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 7ch 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 16ch 3.0T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: ST SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Interventional Coil 1.5T Recalled by Philips North America Llc Due...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Diagnostic Coil 3.0T Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Achieva TX Interventional Coil 3.0T Recalled by Philips North America Llc...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cinnamon Rolls 16.5oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cheese Danish 16.5 oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund