Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,830 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,830 in last 12 months

Showing 1756117580 of 48,330 recalls

DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature-Throid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: WP Thyroid Recalled by RLC Labs Inc. Due to CGMP Deviations: manufactured...

The Issue: CGMP Deviations: manufactured under the same conditions as those found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 25, 2020· RLC Labs Inc.

Recalled Item: Nature Throid Recalled by RLC Labs Inc. Due to Subpotent Drug: FDA analysis...

The Issue: Subpotent Drug: FDA analysis found product to be subpotent

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 25, 2020· Medtronic Vascular

Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...

The Issue: Subsequent failure of catheters in the field and failed quality testing

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2020· Medtronic Vascular

Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...

The Issue: Subsequent failure of catheters in the field and failed quality testing

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista Akaline Phosphatase (ALPI) Flex reagent cartridge -...

The Issue: Low outlier resultsgenerated with Alkaline Phosphatase (ALPI) Flex reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2020· Medtronic Vascular

Recalled Item: Rashkind Balloon Septostomy Catheter Recalled by Medtronic Vascular Due to...

The Issue: Subsequent failure of catheters in the field and failed quality testing

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2020· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM HER-2/neu (H2n) assay Recalled by Siemens Healthcare...

The Issue: Siemens confirmed that the Upper Limit of Normal (ULN) as claimed in the...

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

Class II — Potential Health HazardOngoing