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 67616780 of 48,330 recalls

Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2024· Vyaire Medical

Recalled Item: AirLife Adult Manual Resuscitator Recalled by Vyaire Medical Due to Risk of...

The Issue: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due...

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

Class I — Serious Health HazardOngoing
FoodJanuary 9, 2024· Wegmans Food Markets, Inc.

Recalled Item: Outrageous Oat Cookies packaged in 5pk and also sold in Bulk Recalled by...

The Issue: Product contains undeclared wheat.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Dr Franz Koehler Chemie Gmbh

Recalled Item: Custodiol HTK Solution Recalled by Dr Franz Koehler Chemie Gmbh Due to...

The Issue: Potential for particles to be present in solution.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" Recalled by...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing