CLASS II Device recall · Reported 17 Feb 2021 · FDA Enforcement Report
Na-201sx-4021 Aspiration Needle Vizishot recalled by Aomori Olympus Co
Aomori Olympus is recalling Na-201sx-4021 Aspiration Needle Vizishot, distributed nationwide in the US. The recall was initiated on 4 Jan 2021 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1059-2021
- FDA event ID
- 87074
- Recalling firm
- Aomori Olympus, Kuroishi, N/A
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 4 Jan 2021
- FDA classified
- 5 Feb 2021
- Reported
- 17 Feb 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
- Device type
- Surgical Instruments
Timeline
| 4 Jan 2021 | Recall initiated by company | |
| 5 Feb 2021 | Classified by FDA | +32 days |
| 17 Feb 2021 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
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.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
NA-201SX-4021 ASPIRATION NEEDLE VIZISHOT 21G, model no. NA-201SX-4021 - Product Usage: Used with ultrasound endoscopes for ultrasound guided fine needle aspiration of submucosal and extramural lesions of the tracheobronchial tree and esophagus.
Where it was distributed
US Nationwide distribution.
Questions about this recall
Why was it 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.
Which lots are affected?
01K, 02K, 03K, 04K, 05K, 06K, 07K, 08K, 09K, 0XK, 92K, 93K, 94K, 95K, 96K, 97K, 98K, 99K, 9XK, 9YK, 9ZK, 95V, 96V, 97V, 98V, 99V, 9XV, 9YV, 9ZV, 01V, 02V, 03V, 04V, 05V, 06V, 07V, 08V,09V, 0XV
Where was it sold?
US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
100 other products · FDA event 87074This product is part of a recall event; the main page for the event is Injector Forcemax recalled by Aomori Olympus Co.
More recalls from Aomori Olympus
All 113| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Reusable distal attachments recalled by Aomori Olympus Co | Aomori Olympus | Other | Nationwide |
| Device | CLASS II | Olympus Distal Attachment (in Olympus Disposable EMR Kit) recalled | Aomori Olympus | Other | Nationwide |
| Device | CLASS II | Injector Forcemax Lower recalled by Aomori Olympus Co | Aomori Olympus | Sterility | Nationwide |
| Device | CLASS II | Injector Forcemax Up 2.8mmch recalled by Aomori Olympus Co | Aomori Olympus | Sterility | Nationwide |
| Device | CLASS II | Needlemaster 4MMx Upper recalled by Aomori Olympus Co | Aomori Olympus | Sterility | Nationwide |
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|---|---|---|---|---|---|
| Device | CLASS II | Medline Convenience Kits: IV Start KIT recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing BD ChloraPrep Clear recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: Open Heart Pack, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline convenience kits labeled as: GYN Robotic CDS, Medline Kit recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled | ConMed | Other | Nationwide |