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. 1,043 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,043 in last 12 months

Showing 13541–13560 of 48,330 recalls

Medical DeviceJanuary 28, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated)...

The Issue: If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· B Braun Medical Inc

Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....

The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2022· B Braun Medical Inc

Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....

The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2022· AMS Packaging Inc

Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...

The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 28, 2022· Esupplementsales, LLC

Recalled Item: HARD DAWN Recalled by Esupplementsales, LLC Due to Marketed Without an...

The Issue: Marketed Without an Approved NDA/ANDA: Firm was informed by Amazon that...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 28, 2022· AMS Packaging Inc

Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...

The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 28, 2022· CONAGRA BRANDS

Recalled Item: Wishbone Thousand Island Dressing 15oz. bottle and 24 Recalled by CONAGRA...

The Issue: Undeclared eggs

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 28, 2022· CONAGRA BRANDS

Recalled Item: Wishbone Chunky Blue Cheese Dressing 24oz. bottle Recalled by CONAGRA BRANDS...

The Issue: Undeclared eggs

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2022· Medtronic MiniMed

Recalled Item: MiniMed 630G: MMT-1715 Recalled by Medtronic MiniMed Due to New or...

The Issue: New or replacement insulin pumps are not pre-programmed with basal rates or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· C.R. Bard Inc

Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...

The Issue: There is a potential to leak from the catheter where it connects to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Hologic, Inc

Recalled Item: Panther Fusion Extraction Reagent-X Recalled by Hologic, Inc Due to Failed...

The Issue: Failed stability specifications for reagent kits that may result in false...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· E25Bio, Inc.

Recalled Item: E25Bio COVID-19 Direct Antigen Rapid Test Recalled by E25Bio, Inc. Due to...

The Issue: The Test is not authorized, cleared, or approved by FDA for clinical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 27, 2022· C.R. Bard Inc

Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...

The Issue: There is a potential to leak from the catheter where it connects to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· IN MY BATHROOM LLC

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Integrity Implants Inc.

Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...

The Issue: Potential for weld separation of the Upper Tulip Head component from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Integrity Implants Inc.

Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...

The Issue: Potential for weld separation of the Upper Tulip Head component from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2022· Integrity Implants Inc.

Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...

The Issue: Potential for weld separation of the Upper Tulip Head component from the...

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

Class II — Potential Health HazardOngoing
FoodJanuary 26, 2022· Siren Snacks

Recalled Item: Siren Birthday Cake Protein Bites Recalled by Siren Snacks Due to Undeclared...

The Issue: Undeclared cashews and almond butter allergens

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Jardiance (empagliflozin tablets) Recalled by CARDINAL HEALTHCARE Due to...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 26, 2022· CARDINAL HEALTHCARE

Recalled Item: Asmanex Twisthaler (mometasone furoate inhalation powder Recalled by...

The Issue: CGMP Deviations: Products were exposed to temperatures outside of the...

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

Class II — Potential Health HazardOngoing
Refund