Stryker Corporation: Stryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.

Recall number

Z-1726-2019

Recalling firm

Stryker Corporation

Product

Stryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.

Status

Terminated

Initiated

2019-03-07

Posted

not on file

Terminated

2024-03-08

Reason

The heated tube sets were consistently leaking and detaching from the cassette.

Root cause

Under Investigation by firm

Action

The recalling firm issued letters dated 3/7/2019 via certified mail on 3/7/2019. A second letter dated 3/7/2019 was issued on 4/15/2019 via certified mail to two customers which included an additional lot number for one of the products.

Quantity

32,537 boxes

Distribution

Distribution was nationwide to medical facilities. There was government/military distribution. Foreign distribution was made to Argentina, Brazil, Canada, Chile, Colombia, (EMEA-no specific address/country listed), India, Japan, Latin America (no country listed), Mexico, Saudi Arabia, UAE, and Uruguay.

Lot, serial or model codes

UDI - 07613327055634   Lot numbers: 18G0269, 18H0353, 18K0379 , 56004320, 56004325, 56004329, 56004356, 56004366, 56004373, 56004384, 56004387, 56004426, 56004432, 56004441, 56004443, 56004451, 56004459, 56004461, 56004487, 56004494, 56004502, 56004508, 56004515, 56004518, 56004528, 56004551, 56004565, 56004573, 56004584, 56004600, 56004614, 56004616, 56004624, 56004628, 56004632, 56004681, 56004686, 56004696, 56004704, 56004719, 56004721, 56004735, 56004737, 56004739, 56004748, 56004750, 56004760, 56004771, 56004791, 56004795, 56004809, 56004811, 56004816, 56004818, 56004820, 56004822, 56004826, 56004830, 56004842, 56004844, 56004846, 56004852, 56004881, 56004909, 56004913, 56004919, 56004925, 56004927, 56004929, 56004938, 56004950, 56004955, 56004957, 56004959, 56004970, 56004974, 56004976, 56004995, 56005003, 56005016, 56005018, 56005020, 56005097, 56005099, 56005104, 56005108, 56005128, 56005130, 56005132, 56005139, 56005198, 56005200, 56005206, 56005212, 56005229, 56005232, 56005246, 56005251, 56005267, 56005295, 56005297, 56005301, 56005323, 56005331, 56005339, 56005341, 56005343, 56005351, 56005353, 56005357, 56005360, 56005370, 56005372, 56005374, 56005426, 56005428, 56005440, 56005480, 56005484, 56005486, 56005504, 56005506, 56005508, 56005532, 56005534, 56005544, 56005555, 56005557, 56005588, 56005590, 56005599, 56005613, 56005615, 56005628, 56005631, 56005637, 56005640, 56005642, 56005671, 56005673, 56005686, 56005688, 56005694, 56005697, 56005710, 56005714, 56005717, 56005719, 56005728, 56005730, 56005732, 56005734, 56005749, 56005751, 56005753, 56005763, 56005765, 56005769, 56005772, 56005779, 56005812, 56005827, 56005833, 56005835, 56005837, 56005839, 56005850, 56005852, 56005858, 56005862, 56005874, 56005876, 56005895, 56005897, 56005913, 56005915, 56005933, 56005935, 56005950, 56005954, 56005965, 56005972, 56005974, 56005987, 56006156, 56006191, 56006201, 56006212, 56006216, 56006222, 56006224, 56006235, 56006249, 56006251, 56006268, 56006309, 56006311, 56006313, 56006321, 56006323, 56006325, 56006332, 56006334, 56006346, 56006348, 56006368, 56006372, 56006374, 56006378, 56006411, 56006413, 56006415, 56006430, 56006432, 56006454, 56006471, 56006473, 56006475, 56006491, 56006493, 56006495, 56006497, 56006501, 56006503, 56006506, 56006508, 56006510, 56006512, 56006542, 56006549, 56006554, 56006613, 56006633, 56006637, 56006540.

510(k) numbers

["K063367"]

PMA numbers

not on file

Product code

HIF

Firm FEI

2936485

Firm city

San Jose

Firm state

CA

Firm country

not on file

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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