Product Safety Recalls

Product Recall Tracker

Stryker Medical Division of Stryker Corporation Recall 93317

Description: ProCuity bed series, model number 3009, item number: 3009PX-LE-400.

Stryker Medical Division of Stryker Corporation Recall 93317 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0427-2024
Event ID93317
Event DescriptionProCuity bed series, model number 3009, item number: 3009PX-LE-400.
Product TypeDevices
DistributionDistribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.
Recall ReasonPatient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Device Classification20231213
Device Code InfoUDI-DI (GTIN): 07613327541182. Serial numbers: 2105002838 , 2105002832 , 2202000312 , 2202000286 , 2202000278 , 2202000180 , 2106002241 , 2106001240 , 2107001002 , 2203001053 , 2203001898 , 2112001135 , 2211002054 , 2105002782 , 2210002902 , 2210002890 , 2210002876 , 2210002858 , 2210002848 , 2111001420 , 2206001182
Center Classification Date20231201
Recall Initiation Date20230830
Recalling FirmStryker Medical Division of Stryker Corporation
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.