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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77671

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 26, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Stryker Neurovascular

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 4

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20, Trevo Pro 14 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK32021001

Z-2799-2017
Recall number
Z-2799-2017
Initiated
June 26, 2017
Classification
Class II
Status
Terminated
Recalling firm
Stryker Neurovascular
Quantity
43 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for 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.

Code information

Lot Numbers: QPC20107530, QPC20107745, QPC20107814, QPC20110247

Distribution pattern

nationwide

device · product 2 of 4

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001

Z-2800-2017
Recall number
Z-2800-2017
Initiated
June 26, 2017
Classification
Class II
Status
Terminated
Recalling firm
Stryker Neurovascular
Quantity
63 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for 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.

Code information

Lot Numbers: QPC30107530, QPC30107745, QPC30107814, QPC30110247

Distribution pattern

nationwide

device · product 3 of 4

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK43022001

Z-2801-2017
Recall number
Z-2801-2017
Initiated
June 26, 2017
Classification
Class II
Status
Terminated
Recalling firm
Stryker Neurovascular
Quantity
139 packs

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for 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.

Code information

Lot Numbers: QPC40107530, QPC40107745, QPC40107814, QPC40110247

Distribution pattern

nationwide

device · product 4 of 4

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25, AXS Catalyst 060x132CM - US, EXCELSIOR XT 27 MICROCATHETER, UPN M0033PK62523001 ST 150

Z-2802-2017
Recall number
Z-2802-2017
Initiated
June 26, 2017
Classification
Class II
Status
Terminated
Recalling firm
Stryker Neurovascular
Quantity
48 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for 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.

Code information

Lot Numbers: QXC10107745, QXC10107814, QXC10110247

Distribution pattern

nationwide