Product Alerts & Recalls
|Publish Date||PAR #||Manufacturer||Post Name||Product Type||Model #|
|July 14, 2020||12-20||Dynamic Safety International (DSI)||Dyna-Yard Lanyard recalled due to lack of certification||Fall Protection||FP758116, FP758136, FP758146, FP7591116, FP7591336 and FP7591446|
|July 17, 2020||13-20||Verathon Medical (Canada) ULC||Verathon, Inc. Recalls GlideScope Core One TouchSmart Cable (“OneTouch cable”), Due to partial or complete loss of image during use||Medical Equipment||0800‐0601|
|June 18, 2020||11-20||Lochinvar, LLC||Certain Lochinvar Condensing Gas Boilers and Condensing Gas Combi Boilers recalled due to risk of carbon monoxide poisoning||Gas Boilers||Several|
|May 22, 2020||10-20||Linyi Kingstar Caps and Shoes Co., Ltd.||TAURUS Safety Shoes recalled due to a lack of certification||Safety Footwear||5001|
|May 14, 2020||09-20||2D2C Inc. (OFI Inc., SafePlug)||SafePlug Model 1202 Controlled Duplex-Receptacle recalled due to fire hazard||1202-9962|
|April 23, 2020||08-20||Leviton||Leviton 50-ampere electrical connectors recalled due to electric shock hazard||Several (see recall for list)|
|April 2, 2020||07-20||Stelpro Design||Stelpro Design Recalls Sonoma Wall Fan Heaters Due to Fire Hazard||ASSO & ASSOS Sonoma (Several Models)|
|March 30, 2020||06-20||CME America (Caesarea Medical Electronics Ltd.)||CME America Recalls BodyGuard Infusion Pump System Due to Risk of Over-, and Under-infusion||Medical Equipment||BG 323, BodyGuard 121 Twins, BodyGuard 545 ColorVision, BodyGuard 575 & CMExpress|
|March 6, 2020||05-20||Becton Dickinson (BD) CareFusion 303 Inc.||Becton Dickinson (BD) CareFusion 303 Inc. Recalls Alaris System Infusion Pumps Due to Software and System Errors||Ventilator||8000, 8015, 8100, 8110, 8120|
|February 19, 2020||04-20||ResMed Limited||ResMed Recalls Stellar 100 and 150 Non-invasive and Invasive Ventilators Due to Sound Alarm Failure||Medical Ventilator||Stellar 100 & 150|
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