Recalls / —

—#194871

Product

Various neurology packs

FDA product code

OJG — Neurological Tray

Device class

Class 1

Medical specialty

Neurology

Affected lot / code info

Tray Number, Sterilization Lot, Lot Number, Bag Serial Number 1) LSRLMNEINTC, 2105181, 870211, 63990989 2) LSRSWRSPNC, 2105251, 861211, 63990357 3) LSRLMNEUROG, 2106161, 845211, 44139500 4) LSRSMHNEURE, 2108101, 793211, 44139500 5) LSRNEURCRANIH, 2108171, 776211, 64123199 6) LSRLMNEUROG, 2110011, 730211, 64316283 7) UINR44M, 2104162, 896211, 64033036 8) TNNE17Y, 2109081, 750211, 64224067 9) SLCR80E, 2104262, 884211, 63986071-006 10) GISP04A, 2104293, 881211, 63985242-006 11) FHNE25Y, 2107083, 811211, 64110740-006 12) BHLA24L, 2108253, 763211, 64205048-006 13) CBAC47F, 2109092, 749211, 64209378-006 14) SLCN72B, 2109161, 741211, 64208359-006 15) BHCR54D, 2104132, 901211, 64072795-006 16) BHCR54D, 2104132, 901211, 64072796-006 17) BHCR54D, 2104132, 901211, 64072273-006 18) BHLM30D, 2105111, 874211, 64062457-006 19) BHCR54D, 2105252, 861211, 64063353-006 20) BHLM30D, 2107091, 819211, 64088774-006 21) BHLM30D, 2107091, 819211, 64088775-006 22) BHLM30D, 2107091, 819211, 64088776-006 23) BHCR54D, 2107161, 810211, 64088824-006 24) BHCR54D, 2107161, 810211, 64088823-006 25) BHLM30D, 2108202, 770211, 64001247-006 26) BHLM30D, 2108202, 770211, 64001248-006 27) BHLM30D, 2108202, 770211, 64001249-006 28) BHLM30D, 2108202, 770211, 64001250-006 29) BHCR54D, 2109022, 757211, 63998620-006 30) BHCR54D, 2109022, 757211, 63998619-006 31) BHCR54D, 2109022, 757211, 63998618-006 32) UMNA22B, 2109292, 728211, 64310294-006 33) DVSP33E, 2104302, 884211, 64064626-006 34) MCSP61F, 2107021, 819211, 64128815-006 35) SJSC27F, 2107091, 813211, 44173743-005 36) SANE32G, 2108091, 784211, 44170921-005 37) MCSP61F, 2108091, 785211, 64138850-006

Why it was recalled

Product was exposed to multiple sterilization cycles without validation for multiple exposures.

Root cause (FDA determination)

Process change control

Action the firm took

The recalling firm began notifying customers of the recall beginning June 13, 2022. Customer notification was initially made via email and an "Urgent Medical Device Recall" letter dated June 16, 2022. Customers are asked to review inventory and segregate affected product, which should be identified with the Bag Serial Number. Affected product should be destroyed, with evidence of destruction provided back to the recalling firm. A Field Action Response Form should be completed and returned to angela.bunn@owens-minor.com as soon as possible, even if the customer has no inventory. If you have any questions, please call 816-920-5846.

Recalling firm

Firm

American Contract Systems, Inc.

Address

2610 Ne Industrial Dr, Ste 220, Kansas City, Missouri 64117-2648

Distribution

Distribution pattern

Distribution within the United States to health systems and distributors in AZ, FL, IA, IL, MA, MN, MO, OH, NE, PA, RI, SD, and TX

Timeline

Recall initiated

2022-06-16

Status

—

Source: openFDA Device Recall endpoint. Recall record ID #194871. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.