Recall StatusTerminated
Date Initiated2008-04-29
Date Terminated2012-10-30
Product Quantity783 units
Reason for Recall
A component defect was found in corner castings of the firm's wheeled ambulance stretchers. Some corner castings on the stretchers were found to be over-sized. Using an over-sized cone-shaped hole corner casting with an improperly seated shank pin could put undue stress on the top screw, possibly causing the screw securing a wheel to become loose or break and the wheel to detach from the stretcher
Firm Action
The firm sent an 'Urgent Field Correction' notification letter to their customers, via certified mail on 5/16/2008. The letter instructs the customers to examine all inventory of Model 35A stretchers. The letter also recommends that any identified unit be removed from service until the unit has been inspected by the customer and a field correction completed, if applicable. Once the inspection of the unit(s) has been completed by the customer, they are to contact the firm immediately and inform them of the results of t their inspections. In the event that a casting fails inspection, the customer is instructed to contact Ferno's Technical Support Div. in order to arrange for a casting replacement. To report the results of their inspection(s) or to address any questions or concerns which the customer may have, contact Ferno Technical Support at 1-866-987-3776 or send an email to
[email protected].
Root Cause
Mixed-up of materials/components
Distribution Pattern
The recalled product was distributed to customers in the following location nationwide: AK, AL, AR, CA, CO, CT, DE, FL, GA, HI, IL, IN, KY, LA, MA, MD, ME, MI, MN, MS, NC, NJ, NM, NY, OH, OK, PA, SC, TN, TX, VA, WI, and WV.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.