Data Foundry

Medical device recalls 2013

KIMGUARD Container Filters — Class II medical device recall Z-0995-2013

Terminated recall by Kimberly-Clark Corporation, reported 2013-04-03, distributed in AK, AL, AR, AZ, CA, CO, FL, GA…. Some individual container filter units might contain thin areas that may potentially compromise the ability of

Recall numberZ-0995-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmKimberly-Clark Corporation, Roswell, GA, United States
Recall initiated2013-03-06
Classified2013-03-26
Reported by FDA2013-04-03
Terminated2013-09-16
DistributedAK, AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NM, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, WI
Countries outside the USAU, BE, CA, HK, JP, PT, SG
Reason classessterility
Lot numbersMF1279XXX, MF1284XXX, MF1287XXX, MF1288XXX, MF1294XXX, MF1316XXX, MF2012XXX, MF2055XXX, MF2086XXX, MF2098XXX, MF2115XXX, MF2146XXX, MF2178XXX, MF2188XXX, MF2196XXX, MF2210XXX, MF2228XXX, MF2243XXX, MF2264XXX, MF2271XXX, MF2285XXX, MF2328XXX, MF2338XXX

Product

KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose another medical device that is to be sterilized by a health care provider.

Reason for recall

Some individual container filter units might contain thin areas that may potentially compromise the ability of the filter to maintain a sterile barrier.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0995-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.