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. 2,630 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,630 in last 12 months

Showing 1106111080 of 27,373 recalls

Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...

The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to The...

The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System Recalled by CareFusion 303, Inc. Due to The Alaris PC unit...

The Issue: The Alaris PC unit can display incorrect syringe type and/or syringe sizes....

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY Recalled by...

The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2020· CareFusion 303, Inc.

Recalled Item: BD Alaris System. The EtCO2 module is a capnograph indicated for continuous...

The Issue: Infusion pump component defect may result in interruption of patient monitoring

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Encore Medical, LP

Recalled Item: DJO EMPOWR Tibial Knee Punch Handle Part No. 801-05-040 and Recalled by...

The Issue: There is a potential for the retaining pin of the tibial punch handle to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 2/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 5/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 1 Undyed 36"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 6/0 VL 18" P-10...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

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

Class II — Potential Health HazardOngoing