Stryker Stroke Fast Packs: Carton Sleeve Label Mismatch Risk
Stryker Neurovascular recalls some Stroke Fast Packs due to mismatched carton sleeve labels and physical contents. Affected units include specific lot numbers and model codes. Consumers should check their packaging for the listed identifiers.
Lower-risk recall
Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs were manufactured using a carton sleeve where the pre-printed contents on the back of the sleeve did not match the physical contents of the pack.
Contact the company
What happened, in plain English
Stryker Neurovascular is recalling certain Stroke Fast Packs because the labels on the carton sleeves don't match the actual contents. This mismatch could lead to incorrect medical device use during stroke treatments. Read more at govinfonow.com/recall/73562-stryker-stroke-fast-packs-carton-sleeve-label-mismatch-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/73562-stryker-stroke-fast-packs-carton-sleeve-label-mismatch-risk · Updated September 21, 2026 · FDA enforcement record: FDA #Z-2800-2017
Cite this page
“Stryker Stroke Fast Packs: Carton Sleeve Label Mismatch Risk.” GovInfoNow, updated September 21, 2026. https://govinfonow.com/recall/73562-stryker-stroke-fast-packs-carton-sleeve-label-mismatch-risk. Based on FDA recall #Z-2800-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2800-2017%22&limit=1).
Why it’s dangerous
The carton sleeve labels indicate a different number of devices than what's actually inside the pack. This mismatch could cause incorrect medical device usage during critical stroke procedures.
Who’s affected
Healthcare professionals using the Stroke Fast Packs for stroke treatment in the U.S. are most at risk if they use the recalled units with mismatched labels.
How to tell if you have this one
Check the carton sleeve for the pre-printed contents label. The affected units have specific lot numbers: QPC30107530, QPC30107745, QPC30107814, QPC30110247. The product codes include M0033PK42022001.
- Brand
Stryker Neurovascular- Category
Medical device
All 4 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
nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2799-2017 | Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20, Trevo Pro 14 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK32021001; Lot Numbers: QPC20107530, QPC20107745, QPC20107814, QPC20110247 | 43 packs |
| Z-2800-2017 | Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001; Lot Numbers: QPC30107530, QPC30107745, QPC30107814, QPC30110247 | 63 packs |
| Z-2801-2017 | Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK43022001; Lot Numbers: QPC40107530, QPC40107745, QPC40107814, QPC40110247 | 139 packs |
| Z-2802-2017 | Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25, AXS Catalyst 060x132CM - US, EXCELSIOR XT 27 MICROCATHETER, UPN M0033PK62523001 ST 150; Lot Numbers: QXC10107745, QXC10107814, QXC10110247 | 48 units |
What to do — step by step
Check Carton Sleeve Label
Verify the pre-printed contents on the carton sleeve match the physical devices inside the pack.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3.8 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-2800-2017 (June 26, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2800-2017 to see it in context.
- Plain-language summary written by qwen3:4b on September 21, 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.