Z-0544-03

25 Gauge Hydrodissection Cannula 1'' (25 mm) with U-Shaped Flattened End

Name: Z-0544-03 25 Gauge Hydrodissection Cannula 1'' (25 mm) with U-Shaped Flattened End
Creator: Surgical Specialties Corp
Published: 2002-11-05
License: https://open.fda.gov/license/

Surgical Specialties Corp / initiated 2002-11-05 / Terminated

FDA source

Surgical Specialties Corp began a recall of 25 Gauge Hydrodissection Cannula 1'' (25 mm) with U-Shaped Flattened End on 2002-11-05. The reason FDA records is "The wrong product in the box". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0544-03
Status: Terminated
Initiated: 2002-11-05
Posted: 2003-02-05
Terminated: 2003-07-31
Recalling firm: Surgical Specialties Corp
Product: 25 Gauge Hydrodissection Cannula 1'' (25 mm) with U-Shaped Flattened End
Product code: GEA Cannula, Surgical, General & Plastic Surgery
Reason for recall: The wrong product in the box.
FDA root cause: Other
Action: The domestic account was contacted via fax on 11/8/02 and 12/10/02. The foreign accounts were contacted via email on 11/5-12/02.
Quantity in commerce: 211 units
Distribution: The product was sent to wholesalers in CA, Spain and Australia
Product codes and lots: Model Number of Device: 3425 Catalog Number: 3425 Lot number: MK10190 exp 11/2006

Product code GEA

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)