FDAFDA · Food and drugs·Recall number Z-2800-2017
Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001
Published August 9, 2017 · Recall initiated: June 26, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker Neurovascular
- Distributor
- nationwide
- Lot
- Lot Numbers: QPC30107530, QPC30107745, QPC30107814, QPC30110247
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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