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. 2,506 recalls have been distributed to Delaware in the last 12 months.
Showing 19061–19080 of 27,373 recalls
Recalled Item: OER-Pro Endoscope Reprocessor Recalled by Olympus Corporation of the...
The Issue: New warning requiring Users to conduct duodenoscope precleaning and manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with...
The Issue: It was reported that the secondary locking mechanism, and its corresponding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Modular Handle Triathlon Instruments Recalled by...
The Issue: Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80 Recalled by Edan...
The Issue: Incorrect CO2 readings with some patient monitors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{Align RT Plus} This is used on Recalled by...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Surface Monitoring System{OSMS Recalled by Varian Medical Systems,...
The Issue: Varian Medical Systems has received reports that unintended changes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Inc. Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: Mindray has identified a potential leakage issue with the CO2 Module's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Incorrect...
The Issue: Incorrect values for the volume calculation. Software update VB30B via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# e4001-04 The Anastoclip Clip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anasto AC Closure System and Anasto Universal Clip Remover- Anasto Recalled...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: Analytical...
The Issue: Trigger lock option does not always prevent x-ray generation. Specifically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is...
The Issue: Devices were incorrectly programmed during manufacturing therefore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products HBsAg Controls Recalled by Ortho-Clinical...
The Issue: The signal/cutoff (s/c) results may increase throughout the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...
The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babytherm 8004/8010 Recalled by Draeger Medical, Inc. Due to Risk associated...
The Issue: Risk associated with operating the device in skin temperature mode with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoClip AC 8cm 35 Clips (1 Each} Large REF # Recalled by LeMaitre...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# 4001-00 The Anastoclip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anastoclip AC 8cm 35 Clips (1 Each} Medium REF # Recalled by LeMaitre...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnastoCiip Universal Clip Remover (6 Pack} REF# e4001-00 The Anastoclip...
The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.