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. 1,017 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,017 in last 12 months

Showing 17181–17200 of 48,330 recalls

FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Tsukeyaki Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

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

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Szechuan Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

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

Class III — Low RiskOngoing
Refund
DrugOctober 21, 2020· H & H Remedies, LLC

Recalled Item: White Liniment packaged in a) 1 oz Recalled by H & H Remedies, LLC Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2020· H & H Remedies, LLC

Recalled Item: Union (black) salve packaged in a) 1/8 oz Recalled by H & H Remedies, LLC...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2020· H & H Remedies, LLC

Recalled Item: Vapor Ointment packaged in a) 1/8 oz Recalled by H & H Remedies, LLC Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 20, 2020· Viewray, Inc.

Recalled Item: ViewRay MRIdian Linac System: Model No. 20000 Recalled by Viewray, Inc. Due...

The Issue: There is a potential that components of the receive coil can reach elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2020· Viewray, Inc.

Recalled Item: ViewRay MRIdian System: Model No. 10000 Recalled by Viewray, Inc. Due to...

The Issue: There is a potential that components of the receive coil can reach elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone Recalled by...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.25g - Product Usage: natural bone Recalled...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Geistlich Pharma North America, Inc.

Recalled Item: Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone Recalled...

The Issue: Difficult to expel Geistlich Bio-Oss granules from the pen, resistance could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2020· Mevion Medical Systems, Inc.

Recalled Item: MEVION S250i Recalled by Mevion Medical Systems, Inc. Due to Treatment beam...

The Issue: Treatment beam information disappears on Treatment Console screen while beam...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Covidien Llc

Recalled Item: Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for Recalled...

The Issue: In-house lab observations and customer reports of overheating and/or thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2020· Olympus Corporation of the Americas

Recalled Item: Olympus Ultrasound Endoscope Recalled by Olympus Corporation of the Americas...

The Issue: A new inspection step was added to the cleaning and disinfection section of...

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

Class II — Potential Health HazardOngoing