FDA Medical Device Recalls (openFDA)
PEROUSE MEDICAL: Synthes Inflation System (03.804.4135) Product Usage: Inflation system is used during kyphoplasty or other interventional kyphoplasty or other interventional procedures, to create and monitor pressure In the balloon catheter and pressure In the balloon catheter and to to deflate the balloon catheter
- Recall number
- Z-0877-2015
- Recalling firm
- PEROUSE MEDICAL
- Product
- Synthes Inflation System (03.804.4135) Product Usage: Inflation system is used during kyphoplasty or other interventional kyphoplasty or other interventional procedures, to create and monitor pressure In the balloon catheter and pressure In the balloon catheter and to to deflate the balloon catheter
- Status
- Terminated
- Initiated
- 2014-10-06
- Posted
- 2014-12-29
- Terminated
- 2017-03-24
- Reason
- Additional instructions for use due to inability to raise the pressure above 10 atm during inflation phase may result in an incomplete inflation or delay in procedure
- Root cause
- Device Design
- Action
- Perouse Medical notified Distributors by Safety Alert Letter sent on October 06, 2014 and and October 07, 2014 by e-mail. The letter identified the defective products and lot numbers and provided a description of the malfunction, risk and mitigation statements. US distributors have been requested to provide the required information to their customers. In addition, the firm has updated device instructions for use. The firm is requiring its customer to fill out a safety notice acknowledgement of receipt form.
- Quantity
- 2184 units
- Distribution
- US Nationwide Distribution in the states of AZ and CO.
- Lot, serial or model codes
- Batch numbers: 4041354/4062650/4072586
- 510(k) numbers
- ["K110604"]
- PMA numbers
- not on file
- Product code
- MAV
- Firm FEI
- 3006942524
- Firm city
- Ivry Le Temple
- Firm state
- not on file
- Firm country
- France
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
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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