Penner Manufacturing Transfer Electric Superior right entry, Patient Transfer/Lift System, Models 384000-1. The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to transfer or lift patients under the direct supervision of trained staff.
FDA Recall Z-1916-2011 · Posted 2011-04-08
Recalling FirmPenner Mfg Inc
Recall StatusTerminated
Product CodeFNG
Date Initiated2009-01-19
Date Terminated2011-04-08
Product Quantity8 lifts
Reason for Recall
Incomplete weld on the pillar mounting bracket
Firm Action
The firm, Penner, sent an undated letter flagged "Important Safety Inspection: Action Required" via certified mail on January 19, 2009 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to inspect the Penner Patient Transfer for any missing Welds of the Pillar Mounting Bracket; inspect the areas indicated in the enclosed photos to confirm the bracket is welded on all edges to the main frame of the base; complete the inspection, and complete and return the attached WELD INSPECTION RESULTS OF PENNER PATIENT TRANSFER form via fax to 402 694-5844 or mail to Penner Manufacturing Inc, 102 Grant Street, Aurora, NE 68818, Attn: Quality Assurance Manager. Penner stated in the letter, if welds are not complete (no weld), discontinue use and contact the Quality Assurance Manager at Penner Manufacturing immediately at 402-694-5003.
If you have any questions, contact the Quality Assurance Manager at 402-694-5003.
Root Cause
Employee error
Distribution Pattern
Worldwide distribution: USA and countries including: Canada and Mexico.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.