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. 1,983 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,983 in last 12 months

Showing 59415960 of 27,373 recalls

Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) CATH ANGIOGRAPHY DRAPE PACK...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) STANDARD OB PACK ASCENSION WI...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Limacorporate S.p.A

Recalled Item: .14.800 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...

The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Limacorporate S.p.A

Recalled Item: .14.500 Recalled by Limacorporate S.p.A Due to Due to manufacturing issue,...

The Issue: Due to manufacturing issue, their is a potential for peripheral holes to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Synovo Production

Recalled Item: ACETABULAR FIXATION CUP Recalled by Synovo Production Due to Medical device...

The Issue: Medical device components were marketed without FDA clearance and without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· DeRoyal Industries Inc

Recalled Item: Custom medical procedure packs labeled as: a) OPEN HEART TRACECART Recalled...

The Issue: The outer package seal could be open, or compromised which affects the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2023· Johnson & Johnson Surgical Vision, Inc.

Recalled Item: VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs...

The Issue: Weld protrusion/physical gap between the housing and pack cover, may exceed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V- For airway Recalled...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Endoscope Reprocessor OER-Mini-For use in cleaning and high-level...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Endoscope Reprocessor OER-Pro-For use in cleaning and high-level...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Abiomed, Inc.

Recalled Item: Abiomed 14Fr Low Profile Introducer Set Recalled by Abiomed, Inc. Due to...

The Issue: There was one complaint that the sidearm of the device detached during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Endoscope Reprocessor OER-Elite-For use in cleaning and high-level...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2023· Olympus Corporation of the Americas

Recalled Item: Tracheal Intubation Fiberscope OLYMPUS LF-P- To be used with an Recalled by...

The Issue: Revised OER-Pro, OER-Elite, OER-Mini endoscope reprocessor labeling- the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye Recalled by TELEFLEX LLC Due...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Pilling LOWSLEY PROSTATIC TRACTOR STR Recalled by TELEFLEX LLC Due to There...

The Issue: There are incomplete pre-cleaning instructions within the Instructions for...

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

Class II — Potential Health HazardOngoing