FDA Medical Device Recalls (openFDA)
Shippert Medical Technologies: Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000. Used for fat transfer and liposuction.
- Recall number
- Z-0170-2018
- Recalling firm
- Shippert Medical Technologies
- Product
- Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000. Used for fat transfer and liposuction.
- Status
- Terminated
- Initiated
- 2017-10-20
- Posted
- not on file
- Terminated
- 2018-10-09
- Reason
- Potential breach of sterility of the packaging.
- Root cause
- Packaging process control
- Action
- A n Urgent: Medical Device Recall letter, dated October 20, 2017, was mailed to the user, identifying the affected device and describing the reason for the recall. The letter also provided the risk to health involved and discussed how the user can recognize the failure. Customers were instructed to remove all affected product from their inventory and quarantine them. Additionally, the letter should be forwarded to all necessary staff. Customers are to complete the Recall Response letter within 10 calendar days. Only the affected products listed should be returned per the instructions provided. Questions should be directed to Customer Service at 800-888-8663.
- Quantity
- 56 units
- Distribution
- Worldwide Distribution -- United States, Australia, and Netherlands.
- Lot, serial or model codes
- Lot 12004
- 510(k) numbers
- ["K092482"]
- PMA numbers
- not on file
- Product code
- MUU
- Firm FEI
- 3008719017
- Firm city
- Centennial
- Firm state
- CO
- 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