Z-1420-2018 Class II Ongoing

Recalled by Autochair — Alfreton

FDA device recall Z-1420-2018 was initiated by Autochair on March 7, 2018 and is designated Class II. Reason for recall: Recalling firm was informed that as a result of combination of a weak spring and incorrect alignment of the locking pin for latching the leg positions, product legs folded inwards while lifting a pers… The recall status is ongoing.

Recall Details

Product Type
Devices
Report Date
April 25, 2018
Initiation Date
March 7, 2018
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity

Product Description

Product: Milford Smartbase Model # 9934105 Pride SmartBase Pride product codes: LSMPLCG A & LSMPLCG B

Reason for Recall

Recalling firm was informed that as a result of combination of a weak spring and incorrect alignment of the locking pin for latching the leg positions, product legs folded inwards while lifting a person off a bed and the individual was dropped.

Distribution Pattern

PA, and worldwide

Code Information

All Lots