FDA Medical Device Recalls (openFDA)
Scanlan International Inc: Scanlan Premier Jacobson Micro Scissors, spring style, flat handle, V-neck, 125-degree angled micro fine blades, 6-1/4'', 16 cm. Catalog Number 7007-449.
- Recall number
- Z-1532-05
- Recalling firm
- Scanlan International Inc
- Product
- Scanlan Premier Jacobson Micro Scissors, spring style, flat handle, V-neck, 125-degree angled micro fine blades, 6-1/4'', 16 cm. Catalog Number 7007-449.
- Status
- Terminated
- Initiated
- 2005-07-27
- Posted
- 2005-09-13
- Terminated
- 2006-12-31
- Reason
- Some scissors purchased before May 1, 2005 may not perform properly. They may have a crack in the blade that could break.
- Root cause
- Other
- Action
- Urgent Medical Device Recall letters were sent 07/27/05 to distributors asking them to retrieve affected product from their customers and return it to Scanlan International, Inc., St. Paul, MN. Distributors are asked to complete and return a Return Fax Form by August 4, 2005 to acknowledge receipt of letter.
- Quantity
- 34
- Distribution
- worldwide. Including the United States and countries such as: Austria, Canada, China, Denmark, Finland, Germany, Greece, India, Italy, Japan, Korea, Malaysia, The Netherlands, Switzerland and Taiwan.
- Lot, serial or model codes
- Lot numbers: U7A, U7B, U7C, U7D, V7A, V7B, V7C, V7D, and W7A. The lot numbers are located on the inside shank of the instrument near the fulcrum. Please note: If there is a ''T'' on the inside shank of one of the spring handles, the instrument is not included in this recall.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- DXY
- Firm FEI
- 2126670
- Firm city
- Saint Paul
- Firm state
- MN
- 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