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FDA Medical Device Recalls (openFDA)

Stat Medical Devices, Inc.: Stat (TM) Super-Fine (TM) Pen Needles and Allison Medical, Inc. Sure Comfort Pen Needles with Silicone Tip, for human use with insulin pen injector device to administer insulin subcutaneously.

Recall number
Z-1596-2009
Recalling firm
Stat Medical Devices, Inc.
Product
Stat (TM) Super-Fine (TM) Pen Needles and Allison Medical, Inc. Sure Comfort Pen Needles with Silicone Tip, for human use with insulin pen injector device to administer insulin subcutaneously.
Status
Terminated
Initiated
2009-05-29
Posted
2009-07-24
Terminated
2010-09-07
Reason
Stat Pen Needles with silicone coating have not been cleared by FDA for use with silicone coating which could significantly affect the safety and effectiveness of the device.
Root cause
PMA
Action
An "Urgent: Medical Device Recall Notification" letter dated June 18, 2009 was issued to direct customers requesting return of affected product and requesting they send notification to any customers which may have received the affected product from them. Direct questions about the recall to Stat Medical Devices by calling 1-978-774-1469.
Quantity
6,424,100 total pen needles
Distribution
Worldwide Distribution -- US (CO and Puerto Rico), Canada, and Saudi Arabia.
Lot, serial or model codes
Part # Lot # Exp Date  PNS-100 SBSM-1107-1 11/2012  SBSM-0608-1 06/2013 and  SBSM-1008-1 10/2013;  PNX-100 SBSM-1107-1 11/2012  SBSM-0408-1 04/2013  SBSM-0508-1 05/2013  SBSM-0608-1 06/2013  SBSM-0908-1 09/2013  SBSM-1008-1 10/2013 and  SBSM-1108-1 11/2013;  PNM-100 SBSM-1107-1 11/2012  SBSM-0408-1 04/2013  SBSM-0508-1 05/2013  SBSM-0608-1 06/2013  SBSM-0908-1 09/2013  SBSM-1008-1 10/2013 and  SBSM-1108-1 11/2013;  24-1010 (PNS-100) SBAL-1107-1 11/2012;  24-1215 (PNX-100) SBAL-1107-1 11/2012; and  24-1210 (PNM-100) SBAL-1107-1 11/2012.
510(k) numbers
not on file
PMA numbers
not on file
Product code
FMI
Firm FEI
1000525253
Firm city
Miami
Firm state
FL
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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