Z-2440-2008

500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and Part #M8275071/10 (10...

Name: Z-2440-2008 500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and Part #M8275071/10 (10...
Creator: KCI USA, Inc.
Published: 2008-07-29
License: https://open.fda.gov/license/

KCI USA, Inc. / initiated 2008-07-29 / Terminated / root cause: manufacturing process

FDA source

KCI USA, Inc. began a recall of 500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and Part #M8275071/10 (10 canister pack); products are single use and labeled as... on 2008-07-29. The reason FDA records is "The port on the 500mL InfoV.A.C. Canister that connects to the suction pump tubing was found to be partially or fully occluded with plastic". 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-2440-2008
Status: Terminated
Initiated: 2008-07-29
Posted: 2008-09-20
Terminated: 2009-07-13
Recalling firm: KCI USA, Inc.
Product: 500 mL InfoV.A.C. Canister (without Gel); Part #M8275071/5 (5 canister pack) and Part #M8275071/10 (10 canister pack); products are single use and labeled as STERILE; distributed by Kinetic Concepts, Inc., San Antonio, TX.
Product code: JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered
Reason for recall: The port on the 500mL InfoV.A.C. Canister that connects to the suction pump tubing was found to be partially or fully occluded with plastic.
Root cause tag: manufacturing process
FDA root cause: Equipment maintenance
Action: Urgent - Medical Device Recall letters were sent within the US on 07/29/08 via UPS next day delivery service and a return receipt was maintained to demonstrate delivery of the recall to all consignees. Additionally, firm is sending representatives into accounts which received more than three sales units of canisters and to all foreign consignee locations to facilitate quarantine and replacement of affected stock. Consignees asked to confirm that adequate flow is being delivered and that the dressing is being drawn down for those patients currently using the InfoV.A.C. Canisters. Also, consignees are to locate and quarantine all packaged 500 ml canisters without the green inspection stickers from within the affected lot numbers in their inventory. A KCI Rep will contact them to help facilitate this process. Consignees are to complete and return the Recall Acknowledgement and Inventory Accounting Form. KCI will replace any affected product at their facility and arrange for the return of any affected product.
Quantity in commerce: 79,275 canisters.
Distribution: Worldwide Distribution --- including USA and countries of Austria, Belgium, Denmark, France, Germany, Netherlands, Sweden, and the UK.
Product codes and lots: For M8275071/5: 20063928 For M8275071/10: 20062500, 20063927, 20063927.15108D, 20063930, 20063930.15108D, 20067296, 20067297, 20067298, 20069122, 20069123, 20069123.15108D, 20069124, 20069124.15108D, 20069276, 20071227, 20073941, 20075083, 20075267, 20079189, 20079190, 20079191, 20089714, and 20094198

Product code JCX

K063740Class IIV.a.c. Therapy Systems - Info V.a.c. Therapy Uniy, Model M6257766Kci USA, Inc. / cleared 2007-06-07

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)