Pioneer Surgical Technology Streamline MIS Navigation System Taps Recall: Incompatibility
Pioneer Surgical Technology recalls Streamline MIS Navigation System Taps (catalog numbers 04-CANNDRILL-MDN, 04-CANNTAP-40-MDN, etc.) due to incompatibility with Streamline MIS tap sleeves. Affected units may cause improper function during surgery.
Lower-risk recall
The Streamline MIS Navigation System taps are not compatible with the Streamline MIS tap sleeve.
Contact the company
What happened, in plain English
Pioneer Surgical Technology is recalling Streamline MIS Navigation System Taps with specific catalog numbers because they are not compatible with the Streamline MIS tap sleeve. This incompatibility could lead to improper function during surgical procedures. Read more at govinfonow.com/recall/64305-pioneer-surgical-technology-streamline-mis-navigation-system-taps-recall-incompatibility.
Source Summary by GovInfoNow · govinfonow.com/recall/64305-pioneer-surgical-technology-streamline-mis-navigation-system-taps-recall-incompatibility · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0320-2021
Cite this page
“Pioneer Surgical Technology Streamline MIS Navigation System Taps Recall: Incompatibility.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64305-pioneer-surgical-technology-streamline-mis-navigation-system-taps-recall-incompatibility. Based on FDA recall #Z-0320-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0320-2021%22&limit=1).
Why it’s dangerous
The taps are not compatible with the Streamline MIS tap sleeve, which could result in improper function during surgical procedures. This incompatibility may cause the taps to not work correctly when used with the intended sleeve.
Who’s affected
Surgical professionals using the Streamline MIS Navigation System Taps with the listed catalog numbers and lot numbers are affected. The risk is low as the issue relates to compatibility rather than immediate safety hazards.
How to tell if you have this one
Check for catalog numbers 04-CANNDRILL-MDN, 04-CANNTAP-40-MDN, 04-CANNTAP-45-MDN, 04-CANNTAP-55-MDN, 04-CANNTAP-65-MDN, 04-CANNTAP-75-MDN, 04-CANNTAP-85-MDN, 04-CTAP-TT-65-MDN, 04-S-FINDER-MDN, 05-SCREWINS-CL-MDN, or 05-SIMPDRIVER-MDN. Also check for lot numbers 377520, 371734, 374791, 374792, 373438, 371735, 371736, 377625, 377806, 371737, 372819, 371266, or 371733.
- Brand
Pioneer Surgical Technology- Category
Medical device
What to do — step by step
Check Compatibility
Verify if your Streamline MIS Navigation System Taps are compatible with the Streamline MIS tap sleeve using the catalog numbers and lot numbers listed in the recall.
Where it went and when
Where it was distributed
Distributed in Michigan.
FDA distribution: “Product distributed to Surgalign, a distributor located in Michigan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Michigan.
Recall timeline
FDA terminated this recall 3.7 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-0320-2021 (September 11, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0320-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 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.