Recall Z-1420-2018— Autochair
Class II · Ongoing
Class II FDA medical device recall by Autochair, initiated 2018-03-07. FDA's recall record names no specific 510(k) clearance for this event. Product: Product: Milford Smartbase Model # 9934105 Pride SmartBase Pride product codes: LSMPLCG A & LSMPLCG B. Reason: 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..
- Recalling firm
- Autochair
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2018-03-07
- Firm location
- Alfreton, United Kingdom
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.