Stryker High Flow II Tube Set Recall: Leaking Tubes Detach from Insufflator
Stryker recalls High Flow II Tube Set (REF 0620-040-660) due to consistent leaking and detachment from the PNEUMO SURE High Flow Insufflator, posing a risk of improper use during medical procedures.
Use caution until it’s fixed
The heated tube sets were consistently leaking and detaching from the cassette.
Contact the company
What happened, in plain English
Stryker is recalling a specific tube set used with their PNEUMO SURE High Flow Insufflator because it leaks and detaches from the device. This could lead to improper use during medical procedures if the tube fails unexpectedly. Read more at govinfonow.com/recall/68897-stryker-high-flow-ii-tube-set-recall-leaking-tubes-detach.
Source Summary by GovInfoNow · govinfonow.com/recall/68897-stryker-high-flow-ii-tube-set-recall-leaking-tubes-detach · Updated August 20, 2026 · FDA enforcement record: FDA #Z-1726-2019
Cite this page
“Stryker High Flow II Tube Set Recall: Leaking Tubes Detach from Insufflator.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/68897-stryker-high-flow-ii-tube-set-recall-leaking-tubes-detach. Based on FDA recall #Z-1726-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1726-2019%22&limit=1).
Why it’s dangerous
The heated tube sets consistently leak and detach from the cassette, which could cause the tube to fail during medical procedures. This might lead to improper use of the insufflator, potentially affecting patient safety.
Who’s affected
Medical professionals using the PNEUMO SURE High Flow Insufflator with the recalled tube set are most at risk. Patients receiving procedures with this specific tube set may be affected.
How to tell if you have this one
Check for the product name 'Stryker High Flow II Tube Set' with the reference number 0620-040-660. The lot numbers listed in the recall include many specific codes like 18G0269, 18H0353, and 56004320.
- Brand
Stryker- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- 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.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1726-2019 | Stryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.; 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. | 32,537 boxes |
| Z-1727-2019 | Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-680, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.; UDI - 07613327055641; Lot numbers: 18G0273, 18H0323, 18H0354, 56004327, 56004391, 56004434, 56004478, 56004526, 56004592, 56004665, 56004667, 56004706, 56004708, 56004784, 56004832, 56005325, 56005376, 56005378, 56005380, 56005411, 56005450, 56005459, 56005538, 56005540, 56005633, 56005635, 56005744, 56005790, 56005899, 56005901, 56005989, 56005997, 56005999, 56006142, 56006154, 56006270, 56006340, 56006434, 56006521, 56006527, 56006556, 56006560, 56006606. | 5,089 boxes |
| Z-1728-2019 | Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-690, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.; UDI - 07613327055658; Lot numbers: 56004333, 56004335, 56004337, 56004342, 56004352, 56004375, 56004393, 56004419, 56004421, 56004423, 56004435, 56004445, 56004447, 56004465, 56004481, 56004485, 56004512, 56004520, 56004534, 56004541, 56004575, 56004577, 56004586, 56004597, 56004602, 56004626, 56004630, 56004643, 56004645, 56004649, 56004651, 56004710, 56004723, 56004725, 56004741, 56004752, 56004754, 56004757, 56004782, 56004786, 56004793, 56004836, 56004838, 56004840, 56004850, 56004863, 56004884, 56005075, 56005077, 56005081, 56005083, 56005085, 56005087, 56005089, 56005091, 56005093, 56005110, 56005112, 56005114, 56005116, 56005117, 56005124, 56005126, 56005141, 56005143, 56005145, 56005147, 56005149, 56005164, 56005168, 56005171, 56005173, 56005175, 56005177, 56005186, 56005190, 56005192, 56005194, 56005218, 56005223, 56005230, 56005236, 56005247, 56005253, 56005269, 56005275, 56005292, 56005292, 56005299, 56005310, 56005349, 56005355, 56005362, 56005364, 56005366, 56005368, 56005382, 56005384, 56005397, 56005409, 56005415, 56005417, 56005419, 56005431, 56005433, 56005435, 56005448, 56005463, 56005465, 56005500, 56005502, 56005511, 56005517, 56005519, 56005521, 56005525, 56005550, 56005552, 56005576, 56005578, 56005580, 56005582, 56005619, 56005644, 56005665, 56005680, 56005682, 56005726, 56005738, 56005759, 56005799, 56005808, 56005829, 56005854, 56005856, 56005887, 56005890, 56005909, 56005911, 56005919, 56005929, 56005937, 56005952, 56005970, 56005995, 56006006, 56006008, 56006014, 56006146, 56006148, 56006150, 56006163, 56006185, 56006187, 56006189, 56006210, 56006218, 56006220, 56006242, 56006255, 56006259, 56006261, 56006263, 56006282, 56006284, 56006286, 56006301, 56006303, 56006305, 56006307, 56006317, 56006342, 56006344, 56006376, 56006407, 56006424, 56006426, 56006442, 56006450, 56006463, 56006523, 56006525, 56006574, 56006576, 56006578, 56006601, 56006609, 56006620, 56006622, 56006631, 56006641, 56006643. | 19,083 boxes |
What to do — step by step
Check Product Details
Identify the tube set by its reference number 0620-040-660 and check if it matches the listed lot numbers.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA 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…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 5 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1726-2019 (March 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1726-2019 to see it in context.
- Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.