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. 2,678 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,678 in last 12 months

Showing 41014120 of 48,330 recalls

Medical DeviceOctober 16, 2024· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Positioner. Model Number C-XP-5000Z Recalled by Maquet...

The Issue: Deviations in the manufacturing process created a compromise in the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter AK 98 Dialysis Machine Recalled by Baxter Healthcare Corporation Due...

The Issue: Baxter is aware of several recalls by other manufacturers related to the...

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

Class I — Serious Health HazardOngoing
DrugOctober 15, 2024· Akron Pharma, Inc.

Recalled Item: OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Pacer Implant Pack Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Some of the suture packages within the convenience kits contain the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Open Heart CDS Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Some of the suture packages within the convenience kits contain the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Shoulder Repair Pack-LF Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Some of the suture packages within the convenience kits contain the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2024· Draeger Medical, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600...

The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 15, 2024· Draeger Medical, Inc.

Recalled Item: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500...

The Issue: The Atlan anesthesia workstation either indicated a failure of the piston...

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

Class I — Serious Health HazardOngoing
FoodOctober 11, 2024· Sprouts Farmers Market

Recalled Item: Sprouts Chicken Street Taco Recalled by Sprouts Farmers Market Due to...

The Issue: Sprout Chicken Street Taco 6 Tacos contains cooked chicken that is...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2024· Padagis US LLC

Recalled Item: Triamcinolone Acetonide Cream USP Recalled by Padagis US LLC Due to...

The Issue: Subpotent and Superpotent Drug. Out of specification assay results recorded...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 11, 2024· Karl Storz Endoscopy

Recalled Item: 4.5 x 180 mm Aggressive Cutter Recalled by Karl Storz Endoscopy Due to Due...

The Issue: Due to holes detected in the inner barrier system that may compromise the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively...

The Issue: May Generate Negatively Biased Results When Testing Samples with High...

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

Class II — Potential Health HazardOngoing
DrugOctober 10, 2024· ACCORD HEALTHCARE, INC.

Recalled Item: Cinacalcet Tablets Recalled by ACCORD HEALTHCARE, INC. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2024· ACCORD HEALTHCARE, INC.

Recalled Item: Cinacalcet Tablets Recalled by ACCORD HEALTHCARE, INC. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2024· ACCORD HEALTHCARE, INC.

Recalled Item: Cinacalcet Tablets 30 mg Recalled by ACCORD HEALTHCARE, INC. Due to CGMP...

The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2024· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2024· Hologic, Inc

Recalled Item: BioZorb Marker. Radiographic soft tissue marker. Recalled by Hologic, Inc...

The Issue: Firm received reports of adverse events/complications that include serious...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2024· Philips Medical Systems Technologies Ltd.

Recalled Item: Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to Recalled by...

The Issue: A software issue affecting Philips Vue PACS may cause incorrect ischemic map...

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

Class II — Potential Health HazardOngoing
DrugOctober 9, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Cinacalcet Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Cinacalcet Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to CGMP...

The Issue: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA...

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

Class II — Potential Health HazardOngoing
Refund