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FDA Medical Device Recalls (openFDA)

Medical Action Industries Inc: Medical Action Industries, Venous Access Tray, using BD Q-Syte Luer Access Split Septum (BD #385100)), Part number: 69498.

Recall number
Z-1074-2010
Recalling firm
Medical Action Industries Inc
Product
Medical Action Industries, Venous Access Tray, using BD Q-Syte Luer Access Split Septum (BD #385100)), Part number: 69498.
Status
Terminated
Initiated
2009-11-06
Posted
2010-03-30
Terminated
2011-06-01
Reason
Manufacturing defect may allow air entry into a central venous catheter, possibly resulting in an air embolism.
Root cause
Nonconforming Material/Component
Action
On 11/6/2009 a letter was drafted and sent by email to three (3) Medical Action Industries customers. They were instructed to return the recalled products in inventory to MAI. They further advised, if the product was distributed to notify their customer, inform them of the recall and instruct them to return the affected lots to MAI.
Quantity
4,280 kits
Distribution
Nationwide distribution
Lot, serial or model codes
Part number: 69498, Lot numbers: 62282, 69902, 70350, 70854 and 72108.
510(k) numbers
["K013621"]
PMA numbers
not on file
Product code
FPA
Firm FEI
1030451
Firm city
Arden
Firm state
NC
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

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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

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