FDA Medical Device Recalls (openFDA)
Millipore Corporation: Millipore Millex Syringe Filter Unit, 33 mm Durapore PVDF 0.22um, Sterile, 50 Filters per box. Catalog Number: SLGVM33RS.
- Recall number
- Z-1044-2010
- Recalling firm
- Millipore Corporation
- Product
- Millipore Millex Syringe Filter Unit, 33 mm Durapore PVDF 0.22um, Sterile, 50 Filters per box. Catalog Number: SLGVM33RS.
- Status
- Terminated
- Initiated
- 2009-11-25
- Posted
- 2010-03-10
- Terminated
- 2011-05-23
- Reason
- Membrane integrity defects may allow the passage of viable or non-viable contaminants to pass through the filter.
- Root cause
- Process control
- Action
- Millipore Corporation issued an "Urgent: Medical Device Recall" letter dated November 24, 2009 requesting users to examine inventory and immediately discontinue use and return all affected product to the firm. For further information, contact Millipore Technical Services at 1-800-645-5476.
- Quantity
- 539 Boxes - 50 per box
- Distribution
- Worldwide Distribution -- United States, Japan and Hungary.
- Lot, serial or model codes
- Lot/Serial Number: R8PN37631, Exp: 30th Nov 2011
- 510(k) numbers
- ["K023892"]
- PMA numbers
- not on file
- Product code
- BSN
- Firm FEI
- 2244894
- Firm city
- Billerica
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28