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Lower risk Medical device recall · FDA · Published August 14, 2017

Deerfield Imaging Starburst Adaptor Thumb Screw Recall: Incorrect Thread Hazard

Deerfield Imaging recalls Starburst adaptor thumb screws with serial numbers 10006657-10006726 due to incorrect thread design. This may cause improper installation and potential safety issues.

🇺🇸 FDA recall #Z-3211-2017Medical deviceDeerfield Imaging ›
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Recalling firmDeerfield Imaging5101 Shady Oak Rd S · Minnetonka, MN 55343-4100
✎ GovInfoNow plain-language explainer

What happened, in plain English

Deerfield Imaging is recalling Starburst adaptor thumb screws with specific serial numbers because they have an incorrect thread design. This could lead to improper installation and potential safety issues if used incorrectly. Read more at govinfonow.com/recall/73140-deerfield-imaging-starburst-adaptor-thumb-screw-recall-incorrect-thread-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/73140-deerfield-imaging-starburst-adaptor-thumb-screw-recall-incorrect-thread-hazard · Updated September 18, 2026 · FDA enforcement record: FDA #Z-3211-2017

Cite this page

“Deerfield Imaging Starburst Adaptor Thumb Screw Recall: Incorrect Thread Hazard.” GovInfoNow, updated September 18, 2026. https://govinfonow.com/recall/73140-deerfield-imaging-starburst-adaptor-thumb-screw-recall-incorrect-thread-hazard. Based on FDA recall #Z-3211-2017 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3211-2017%22&limit=1).

Why it’s dangerous

The thumb screws have an incorrect thread design, which can lead to improper installation. This may cause the screws to not function as intended, potentially leading to safety issues if used incorrectly.

Who’s affected

Owners of the Starburst adaptor thumb screws with serial numbers 10006657 through 10006726 are affected. Users who install these screws incorrectly may face safety issues.

How to tell if you have this one

Check the serial numbers on the Starburst adaptor thumb screws: 10006657, 10006658, 10006725, 10006660, 10006726, and 10006659. These specific serial numbers are part of the recall.

  • Brand
    Deerfield Imaging
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Serial Numbers

    Verify the serial numbers on the Starburst adaptor thumb screws to see if they match the recalled numbers: 10006657, 10006658, 10006725, 10006660, 10006726, 10006659.

Where it went and when

Where it was distributed

Distributed in 3 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “IL, OR, PA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Oregon, Pennsylvania.

Recall timeline

FDA terminated this recall 9 months after the firm started it.

1. Firm started the recall: Aug 14, 201712. FDA classified it Class II: Sep 22, 201723. Published in FDA’s Enforcement Report: Oct 4, 201734. FDA terminated the recall: May 29, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. 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-3211-2017 (August 14, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3211-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on September 18, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA