FDA Medical Device Recalls (openFDA)
The Raymond Corporation: Raymond Laser alignment guide - Model #1096597/002 Red Laser. Intended to assist operators in performing material handling activities such as storing and retrieving pallets and material in and on racking projecting a line onto a pallet or other material storage medium for assisting the operator in determining the position of the powered industrial truck forks with respect to load.
- Recall number
- Z-0485-2012
- Recalling firm
- The Raymond Corporation
- Product
- Raymond Laser alignment guide - Model #1096597/002 Red Laser. Intended to assist operators in performing material handling activities such as storing and retrieving pallets and material in and on racking projecting a line onto a pallet or other material storage medium for assisting the operator in determining the position of the powered industrial truck forks with respect to load.
- Status
- Terminated
- Initiated
- 2011-11-28
- Posted
- 2012-01-11
- Terminated
- not on file
- Reason
- Raymond shipped a laser alignment guide as an option on its powered industrial trucks from February 2, 2010 through April 21, 2011, but was not aware of its obligation under 21 C.F.R. 1010.2 and 1010.3 to certify and label.
- Root cause
- Radiation Control for Health and Safety Act
- Action
- Raymond will be initiating a Field Campaign to ensure that all customers with Alignment Guides have the confirmatory laser caution decals and manufacturer label, an updated installation and service manual, the operator instructions, and informational brochure. This campaign will be performed at no cost to Raymond's dealers and customers, and will include documenting the laser serial number for each truck configured with an Alignment Guide for product traceability.
- Quantity
- 493 total
- Distribution
- Nationwide Distribution
- Lot, serial or model codes
- Model #1096597/002
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- RER
- Firm FEI
- 1000255174
- Firm city
- Greene
- Firm state
- NY
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28