Z-2467-2010

Braun wheelchair lift, model NL, Braun Corporation, Winamac, IN A wheelchair lift for motor vehicles

Name: Z-2467-2010 Braun wheelchair lift, model NL, Braun Corporation, Winamac, IN A wheelchair lift for motor vehicles
Creator: The Braun Corporation
Published: 2007-08-15
License: https://open.fda.gov/license/

The Braun Corporation / initiated 2007-08-15 / Terminated / root cause: design

FDA source

The Braun Corporation began a recall of Braun wheelchair lift, model NL, Braun Corporation, Winamac, IN A wheelchair lift for motor vehicles on 2007-08-15. The reason FDA records is "The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2467-2010
Status: Terminated
Initiated: 2007-08-15
Posted: 2010-09-22
Terminated: 2011-05-12
Recalling firm: The Braun Corporation
Product: Braun wheelchair lift, model NL, Braun Corporation, Winamac, IN A wheelchair lift for motor vehicles.
Product code: ING Elevator, Wheelchair, Portable
Reason for recall: The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured.
Root cause tag: design
FDA root cause: Device Design
Action: The Braun Corporation issued a Service Bulletin 34273 entitled "Lift Threshold Sensitivity Bulletin 34273 on October 2007. Braun Corporation also sent a "Safety Recall" letter to the Braun lift owner and letters to all customers on or about August 15, 2007. The letters described the product, problem and the action to be taken by the customer. The customers were instructed to notify the National Highway Traffic Safety Administration (NHTSA) and conduct a safety recall if they used recalled lifts as original equipment in a system or vehicle that they built; ensure that any associated customers are notified to discontinue the use of their vehicles until they schedule a repair, and verify the threshold warning system is within the NHTSA specification. The customers were informed to contact the NHTSA with questions by calling the Vehicle Safety Hotline at 1-888-327-4236 or go to http//www.safercar.gov. If they have any problem obtaining the needed repair or wish to schedule service with an approved Braun technician, contact the Braun Corporation Product Support at 1-800-946-7513.
Quantity in commerce: 8,356
Distribution: Worldwide distribution
Product codes and lots: model year 2005-2006.

Product code ING

K952946Class IIVangator IICrow River Industries, Inc. / cleared 1995-11-29

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)