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. 2,661 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,661 in last 12 months

Showing 65816600 of 48,330 recalls

DrugFebruary 2, 2024· Bausch Health Companies, Inc.

Recalled Item: Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1 Recalled by...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with Recalled by...

The Issue: Pack and pouch label is missing the manufacturing and expiration date.

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

Class II — Potential Health HazardOngoing
FoodFebruary 1, 2024· House of Coffee Beans, Inc

Recalled Item: Coffee 5 pound bags Recalled by House of Coffee Beans, Inc Due to potential...

The Issue: potential allergen contact with almonds, pecans and coconut.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 1, 2024· Integrity Products

Recalled Item: RAM IT Recalled by Integrity Products Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· Integrity Products

Recalled Item: To the Moon Capsules Recalled by Integrity Products Due to Undeclared Sildenafil

The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2024· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Recalled Item: TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid Recalled by...

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
DrugFebruary 1, 2024· NATCO Pharma Limited

Recalled Item: Lansoprazole Delayed-Release Capsules USP Recalled by NATCO Pharma Limited...

The Issue: CGMP Deviations: Inadequate induction sealing on bottles, capsules were...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 1, 2024· Amerisource Health Services LLC

Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Amerisource Health Services...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 1, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis: MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinets, running affected software, and Windows 10...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: Wash station: M1000 Wash Station Assembly & DITI Slide Recalled by Abbott...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Technicality Inc.

Recalled Item: Trumpet Recalled by Technicality Inc. Due to The Ring on the Trump Needle...

The Issue: The Ring on the Trump Needle Guide can detach when excessive pressure is...

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

Class II — Potential Health HazardOngoing
FoodJanuary 30, 2024· Reser's Fine Foods, Inc.

Recalled Item: The recalled Reser's Amish Macaroni Salad was packaged in a Recalled by...

The Issue: Undeclared Wheat. The recalled Reser's Amish Macaroni Salad was packaged in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: Equate Lubricant Eye Ointment (Mineral Oil 42.5% Recalled by Brassica Pharma...

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
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: CVS Health Lubricant Eye Ointment (Mineral oil 31.9% Emollient Recalled by...

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
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: Lubricant PM Ointment (Mineral Oil 42.5% and White Petrolatum 57.3%)...

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
DrugJanuary 30, 2024· Brassica Pharma Pvt Ltd

Recalled Item: Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9% Recalled by Brassica...

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