Z-0326-2017 Class II Terminated
FDA device recall Z-0326-2017 was initiated by Hill-Rom, Inc. on August 9, 2016 and is designated Class II. Reason for recall: Ceiling Bracket 71 was shipped with a larger center hole. A potentially hazardous situation exists that if the Ceiling Bracket 71 with a larger center hole is used for a concrete ceiling Ultra Sys… The recall status is terminated (terminated March 24, 2017). Affected quantity: 188.
Recall Details
- Product Type
- Devices
- Report Date
- November 9, 2016
- Initiation Date
- August 9, 2016
- Termination Date
- March 24, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 188
Product Description
Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likorall 200, 242, 243, 250, and LikoGuard L and XL.
Reason for Recall
Ceiling Bracket 71 was shipped with a larger center hole. A potentially hazardous situation exists that if the Ceiling Bracket 71 with a larger center hole is used for a concrete ceiling Ultra System installation with the M8 screw and the safe working load is exceeded, the system could fall.
Distribution Pattern
WA NC OH PA MI Australia Sweden
Code Information
manufacturing date between Dec 01, 2015- Apr 14, 2016