Z-1537-05

SCANLAN Premier Jacobson Micro Scissors, spring style, round handle, 90-degree angled nano blades, 6-12''...

Name: Z-1537-05 SCANLAN Premier Jacobson Micro Scissors, spring style, round handle, 90-degree angled nano blades, 6-12''...
Creator: Scanlan International Inc
Published: 2005-07-27
License: https://open.fda.gov/license/

Scanlan International Inc / initiated 2005-07-27 / Terminated

FDA source

Scanlan International Inc began a recall of SCANLAN Premier Jacobson Micro Scissors, spring style, round handle, 90-degree angled nano blades, 6-12'', 16.5 cm. Catalog no. 7007-596 on 2005-07-27. The reason FDA records is "Some scissors purchased before May 1, 2005 may not perform properly. They may have a crack in the blade that could break". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1537-05
Status: Terminated
Initiated: 2005-07-27
Posted: 2005-09-13
Terminated: 2006-12-31
Recalling firm: Scanlan International Inc
Product: SCANLAN Premier Jacobson Micro Scissors, spring style, round handle, 90-degree angled nano blades, 6-12'', 16.5 cm. Catalog no. 7007-596.
Product code: DXY Implantable Pacemaker Pulse-Generator
Reason for recall: Some scissors purchased before May 1, 2005 may not perform properly. They may have a crack in the blade that could break.
FDA 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 in commerce: 15
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.
Product codes and lots: 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.

Product code DXY

The FDA recall record names no cleared device, and no clearance has been matched to it.

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)