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. 2,655 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,655 in last 12 months

Showing 80818100 of 48,330 recalls

Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Airway Mobilescope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-MR1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-C1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton C1/T1/MR1 Recalled by Hamilton Medical, Inc. Due to Degrading...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Zimmer, Inc.

Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...

The Issue: The outer package labeling and product etch are for a Size 6, however, the...

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

Class II — Potential Health HazardOngoing
FoodJuly 25, 2023· The Sausage Maker, Inc.

Recalled Item: The Sausage Maker Instacure #1 Recalled by The Sausage Maker, Inc. Due to...

The Issue: Contains Sodium Nitrite recalled for potential metal contamination

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 25, 2023· SenTec AG

Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...

The Issue: During rework of components during the manufacturing process, an additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Diversatek Healthcare

Recalled Item: ZVU Functional GI Software Recalled by Diversatek Healthcare Due to GI...

The Issue: GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact...

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

Class III — Low RiskOngoing
Medical DeviceJuly 25, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Medtronic Navigation, Inc.-Littleton

Recalled Item: The O-arm O2 Imaging System is a mobile x-ray system Recalled by Medtronic...

The Issue: Ground cable installed incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Cook Vandergrift, Inc.

Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...

The Issue: Sterility of device may be compromised due to breach of the chevron seal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Smith & Nephew, Inc.

Recalled Item: TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT...

The Issue: A complaint was received indicating that a package contained a TRIGEN...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Smith & Nephew, Inc.

Recalled Item: TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT...

The Issue: A complaint was received indicating that a package contained a TRIGEN...

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

Class II — Potential Health HazardOngoing
DrugJuly 21, 2023· The Ritedose Corporation

Recalled Item: Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Recalled...

The Issue: CGMP deviation: product released prior to supplier approval.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2023· Aurobindo Pharma USA Inc.

Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...

The Issue: cGMP deviations: Batch was released prior to approval.

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

Class II — Potential Health HazardOngoing
Refund