Z-1002-2011

Stryker Endoscopy, Infravision Esophageal Kit, Model Numbers: 220180548, 220180540, 220180560

Name: Z-1002-2011 Stryker Endoscopy, Infravision Esophageal Kit, Model Numbers: 220180548, 220180540, 220180560
Creator: Stryker Endoscopy
Published: 2010-05-11
License: https://open.fda.gov/license/

Stryker Corp. / initiated 2010-05-11 / Terminated / root cause: design

FDA source

Stryker Endoscopy began a recall of Stryker Endoscopy, Infravision Esophageal Kit, Model Numbers: 220180548, 220180540, 220180560 on 2010-05-11. The reason FDA records is "The silicone sheath component of the product detaches from the catheter upon removal of the e-kit from the body". 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-1002-2011
Status: Terminated
Initiated: 2010-05-11
Posted: 2011-02-01
Terminated: 2011-02-01
Recalling firm: Stryker Corp.
Product: Stryker Endoscopy, Infravision Esophageal Kit, Model Numbers: 220180548, 220180540, 220180560
Product code: FAT Bougie, Esophageal, And Gastrointestinal, Gastro-Urology
Reason for recall: The silicone sheath component of the product detaches from the catheter upon removal of the e-kit from the body.
Root cause tag: design
FDA root cause: Device Design
Action: On 5/11/10, Stryker Endoscopy initiated the recall notification letters explaining the reason for the recall and requesting the product be returned.
Quantity in commerce: 4125
Distribution: Nationwide and 3 foreign consignees (Canada, Singapore and Switzerland).
Product codes and lots: PSTR010710-1, PSTR081109-1, PSTR081109-2, PSTR081209-1, PSTR081309-2, PSTR082109-1, PSTR082709-1, PSTR082809-1, PSTR090809-1, PSTR091809-1, PSTR091809-2, PSTR092409-1, PSTR100309-1, PSTR100909-1, PSTR110609-1, PSTRI20709-2, PSTR121809-1, PSTR122209-1, STR021009-8R, STR022709-1R, STR022709-2R, and STR041709-4R

Product code FAT

K983220Class IIStryker Infravision Esophageal KitStryker Endoscopy / cleared 1999-06-04

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)