Reported Feb 17, 2021 · Terminated
NA-201SX-4022-B ASPIRATION NEEDLE ViziShot 22G, model no. NA-201SX-4022-B - Product Usage: Used with ultrasound…
Aomori Olympus Co., Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aomori Olympus Co., Ltd. · 2 Chome 248-1 · Kuroishi, N/A · N/A
Is this the product you have?
- NA-201SX-4022-B ASPIRATION NEEDLE ViziShot 22G, model no
- NA-201SX-4022-B - Product UsageUsed with ultrasound endoscopes for ultrasound guided fine needle aspiration of submucosal and extramural lesions of the tracheobronchial tree and esophagus
- Lot codes and dates
07K08K92K93K95V96V97V98V99V9XV9YV9ZV01V02V03V04V05V06V07V08V09V0XV
- Amount recalled
- 7,400,000 (globally); 260,395 (US)
This recall covers 111 products
The agency filed one notice per product. You are reading one of them; the other 110 are below.
98 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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