Z-0405-2010

Intelligent Reload, 45 mm Blue, product code iR45B; Intelligent Reload, 45 mm Green, product code iR45G...

Name: Z-0405-2010 Intelligent Reload, 45 mm Blue, product code iR45B; Intelligent Reload, 45 mm Green, product code iR45G...
Creator: Surgical Devices/Covidien
Published: 2009-09-23
License: https://open.fda.gov/license/

Medtronic, Inc. / initiated 2009-09-23 / Terminated / root cause: manufacturing process

FDA source

Surgical Devices/Covidien began a recall of Intelligent Reload, 45 mm Blue, product code iR45B; Intelligent Reload, 45 mm Green, product code iR45G; Intelligent Reload Mid Cut 45mm Blue, product code... on 2009-09-23. The reason FDA records is "Lack of assurance that products were manufactured under GMPs. This action is being undertaken due to certain products potentially exhibiting compromised staple formation or cutting which in some instances may result in...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0405-2010
Status: Terminated
Initiated: 2009-09-23
Posted: 2009-11-23
Terminated: 2010-03-08
Recalling firm: Medtronic, Inc.
Product: Intelligent Reload, 45 mm Blue, product code iR45B; Intelligent Reload, 45 mm Green, product code iR45G; Intelligent Reload Mid Cut 45mm Blue, product code iR45MB; Intelligent Reload Mid Cut 45mm Green, product code iR45MG; Intelligent Reload, 45 mm, Vascular, product code iR45V; Intelligent Reload, 60 mm Blue, product code iR60B; Intelligent Reload, 60 mm Green, product code iR60G; Intelligent Reload Mid Cut 60mm Blue, product code iR60MB; Intelligent Reload Mid Cut 60mm Green, product code iR60MG; Intelligent Reload, 60 mm Blue No Knife, product code iR60B4.
Product code: GDW Staple, Implantable
Reason for recall: Lack of assurance that products were manufactured under GMPs. This action is being undertaken due to certain products potentially exhibiting compromised staple formation or cutting which in some instances may result in extended surgical time for the patient.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: The recalling firm issued an Urgent Medical Device Recall letter dated 9/22/09 to all customers. The letter informed customers that Covidien acquired PMI, about the problem with the products, and about the need to return any products remaining inventory. Customers were asked to return the entire inventory of Power Medical Interventions product, regardless of its expiration date. This process can be initiated by contacting Power Medical Innovations customer service at 1-866-769-3763.
Quantity in commerce: 21,958units
Distribution: The products were shipped medical facilities nationwide. The product was also shipped to distributors in Canada, Japan, Germany, Ireland, Italy, Spain, Taiwan, Belgium, Sweden, Netherlands, Israel, Portugal, India, Austria, Turkey, and Greece.
Product codes and lots: all codes

Product code GDW

K071708Class III45, I45s, I60, and I60sPower Medical Interventions, Inc. / cleared 2007-09-27

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 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)