FDA Medical Device Recalls (openFDA)
Smiths Medical PM, Inc.: Smiths Pneupac babyPAC portable ventilator, model 100. Designed for use by qualified medical caregivers, paramedics and other trained personnel, for hospital, emergency and transport ventilation of patients during respiratory distress or insufficiency.
- Recall number
- Z-0436-06
- Recalling firm
- Smiths Medical PM, Inc.
- Product
- Smiths Pneupac babyPAC portable ventilator, model 100. Designed for use by qualified medical caregivers, paramedics and other trained personnel, for hospital, emergency and transport ventilation of patients during respiratory distress or insufficiency.
- Status
- Terminated
- Initiated
- 2005-12-05
- Posted
- 2006-01-24
- Terminated
- 2006-12-26
- Reason
- A potential safety related problem associated with the Pnuepac babyPac Ventilator model 100 has been discovered in that the interface between the air input hose and the air input fitting may leak, and if tightened too much, the air input fitting may loosen when trying to remove the air hose.
- Root cause
- Other
- Action
- Consignees were provided a Safety Action Bulletin, number 05-SAB05, dated 12/05/05. This requests that affected devices be quarantined, Smiths Medical be contacted and devices ultimately be returned to Smiths Medical Pm, Inc. Service Departmentfor repair.
- Quantity
- 44
- Distribution
- CA, CO, IN,MN, NY, PA, TN, TX
- Lot, serial or model codes
- 0504244, 0505158, 0506211, 0506218, 0506242, 0506248, 0506254, 0506265, 0506283, 0506289, 0506321, 0506346, 0506358, 0507127, 0507139, 0507234, 0507235, 0507236, 0507248, 0507249, 0507265, 0508173, 0508174, 0508195, 0508196, 0508197, 504227, 504254, 505139, 505142, 505145, 505257, 505271, 505276, 505286, 506155, 506158, 506169, 506171, 506194, 506233, 506241, 506343, 507317
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- BTL
- Firm FEI
- 2183502
- Firm city
- Waukesha
- Firm state
- WI
- 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