FDA Medical Device Recalls (openFDA)
Kendall Healthcare Products Co: Kendall MONOJECT MAGELLAN 12cc Syringe with Safety Needle 20G X 1.5 inch Product Number: 5551822015
- Recall number
- Z-0108-05
- Recalling firm
- Kendall Healthcare Products Co
- Product
- Kendall MONOJECT MAGELLAN 12cc Syringe with Safety Needle 20G X 1.5 inch Product Number: 5551822015
- Status
- Terminated
- Initiated
- 2004-10-08
- Posted
- 2004-11-02
- Terminated
- 2012-05-15
- Reason
- Needle cannula may separate from the hub during use
- Root cause
- Other
- Action
- Recall letters requesting product return were mailed to all customers on October 8, 2004
- Quantity
- not on file
- Distribution
- Nationwide
- Lot, serial or model codes
- Lot numbers in the range of 406100 through 424600 (inclusive)
- 510(k) numbers
- ["K012736"]
- PMA numbers
- not on file
- Product code
- FMI
- Firm FEI
- 1282497
- Firm city
- Mansfield
- 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