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. 2,694 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,694 in last 12 months

Showing 25412560 of 13,379 recalls

DrugAugust 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2022· HERON THERAPEUTICS, INC.

Recalled Item: Zynrelef (bupivacaine and meloxicam) Recalled by HERON THERAPEUTICS, INC....

The Issue: Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion 0.05% Recalled by CIPLA Due to Lack of...

The Issue: Lack of Assurance of Sterility: Complaints received of defective container...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 1, 2022· Akorn, Inc

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Akorn, Inc Due to Defective...

The Issue: Defective Container: Product has incomplete induction seals.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2022· Edgewell Personal Care Brands, LLC

Recalled Item: Banana Boat hair & scalp defense Recalled by Edgewell Personal Care Brands,...

The Issue: Chemical contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 28, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Rifampin Capsules Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations:OOS result was observed in 1-Methyl-4-Nitroso Piperazine...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2022· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Divalproex Sodium Extended Release Tablets Recalled by Amneal...

The Issue: Failed dissolution specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2022· Amerisource Health Services LLC

Recalled Item: Azacitidine for Injection Recalled by Amerisource Health Services LLC Due to...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugJuly 25, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Pantoprazole Sodium for Delayed-Release Oral Suspension*40 mg* suspension in...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2022· SterRx, LLC

Recalled Item: fentaNYL Citrate in 0.9% Sodium Chloride Recalled by SterRx, LLC Due to Lack...

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
DrugJuly 25, 2022· SterRx, LLC

Recalled Item: FentaNYL Citrate in 0.9% Sodium Chloride 1 mg per 100 mL (10 mcg per mL) IV...

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
DrugJuly 22, 2022· Distributor RFR, LLC.

Recalled Item: SANGTER Energy Supplement Capsules Recalled by Distributor RFR, LLC. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 21, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: below specification limits for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: below specification limits for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2022· Ultra Supplement LLC

Recalled Item: SUSTANGO (Pendenadril Tytrate Blend) Capsules Recalled by Ultra Supplement...

The Issue: Marketed Without an Approved NDA/ANDA: Analytical testing showed the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 20, 2022· AVKARE Inc.

Recalled Item: Lamotrigine Tablets Recalled by AVKARE Inc. Due to Labeling: Label Error on...

The Issue: Labeling: Label Error on Declared Strength

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

Class III — Low RiskOngoing
Refund
DrugJuly 19, 2022· Strides Pharma Inc.

Recalled Item: Prednisone Tablets USP Recalled by Strides Pharma Inc. Due to Presence of...

The Issue: Presence of foreign tablet: 2.5 mg tablet in a 20 mg bottle of Prednisone...

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
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 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