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Lower risk Medical device recall · FDA · Published December 22, 2021

Oscor Destino Twist 14F: Potential hub separation hazard

Oscor recalls Destino Twist 14F (Guidestar 14F) models with possible hub separation risk. Affected units include specific model numbers and lots. No remedy stated in recall.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0646-2022Medical deviceOscor ›
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Contact the company

Recalling firmOscor Inc.3816 Desoto Blvd · Palm Harbor, FL 34683-1618
✎ GovInfoNow plain-language explainer

Oscor is recalling Destino Twist 14F (also called Guidestar 14F) devices due to a potential separation between the threaded hub and cap at one end. This could lead to the device becoming unstable or malfunctioning, though the recall does not specify serious injury risks or a fix. Read more at govinfonow.com/recall/61387-oscor-destino-twist-14f-potential-hub-separation-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/61387-oscor-destino-twist-14f-potential-hub-separation-hazard · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0646-2022

Cite this page

“Oscor Destino Twist 14F: Potential hub separation hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61387-oscor-destino-twist-14f-potential-hub-separation-hazard. Based on FDA recall #Z-0646-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0646-2022%22&limit=1).

Oscor Inc. recalled Destino Twist 14F and Guidestar 14F devices due to potential separation of the threaded hub and cap, the FDA said on Dec. 22, 2021. Owners should contact Oscor for a replacement.

How to tell if you have it

  • Destino Twist 14F (Model DST1405525), Lot PQOC13475
  • Guidestar 14F (Model D141103), Lots DP14073, DP14072, DP14071, DP13834, DP13828, DP13827, DP13811, DP13812, PQOC12995, PQOC12632, PQOC12633, PQOC12345, PQOC12330
  • UPC 00885672010911, UPC 00885672011123

The hazard

There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.

Context

GovInfoNow's records show Oscor Inc. has three other recalls on record since Sept. 26, 2018. Other recent recalls of similar products include Synthes 2.4V TAP CORTEX SCREW Recall (Feb. 25, 2026).

How to tell if you have this one

Check for model numbers DST1405525 (Destino Twist 14F) or D141103 (Guidestar 14F) with specific lots listed in the recall. The recall includes detailed UDI codes for each lot.

  • Brand
    Oscor
  • Product
    Destino Twist 14F (also branded as Guidestar 14F)
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Model and Lot

    Identify your device's model number and lot code from the recall list to confirm if it is affected.

Where it went and when

Where it was distributed

Distributed in Pennsylvania and Tennessee.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: 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: yesTNNorth 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: “Distribution to TN and PA in USA OUS distribution to Czech Republic” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Pennsylvania, Tennessee.

Recall timeline

FDA published this recall 2 months after the firm started it.

1. Firm started the recall: Dec 22, 202112. FDA classified it Class II: Feb 17, 202223. Published in FDA’s Enforcement Report: Feb 23, 2022320212022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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-0646-2022 (December 22, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0646-2022 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.
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