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Lower risk Medical device recall · FDA · Published November 11, 2019

Medicrea Universal Counter Torque Recall: Incompatible with Pass TULIP Spinal System

Medicrea International recalls Universal Counter Torque (A22020500) due to incompatibility with Pass TULIP [Spinal] System nut drivers. Affected units may cause improper installation.

🇺🇸 FDA recall #Z-1234-2020Medical deviceMedicrea International ›
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Recalling firmMedicrea International5389 Route De Strasbourg, Vancia · Rillieux La Pape, France
✎ GovInfoNow plain-language explainer

What happened, in plain English

Medicrea International is recalling its Universal Counter Torque (A22020500) because it is incompatible with the Pass TULIP [Spinal] System's nut driver (A22020220). This could lead to improper installation if used together. Read more at govinfonow.com/recall/66538-medicrea-universal-counter-torque-recall-incompatible-with-pass-tulip-spinal.

Source Summary by GovInfoNow · govinfonow.com/recall/66538-medicrea-universal-counter-torque-recall-incompatible-with-pass-tulip-spinal · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1234-2020

Cite this page

“Medicrea Universal Counter Torque Recall: Incompatible with Pass TULIP Spinal System.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66538-medicrea-universal-counter-torque-recall-incompatible-with-pass-tulip-spinal. Based on FDA recall #Z-1234-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1234-2020%22&limit=1).

Why it’s dangerous

The Universal Counter Torque (A22020500) is designed to be incompatible with the Pass TULIP [Spinal] System's nut driver (A22020220). Using them together could result in improper installation, potentially causing issues with spinal surgery equipment.

Who’s affected

Users of the Pass TULIP [Spinal] System who have the Universal Counter Torque (A22020500) model are affected. Medical professionals using this specific combination are most at risk.

How to tell if you have this one

Check for the model number A22020500 on the Universal Counter Torque. This product was sold with the Pass TULIP [Spinal] System and has a lot number of 19H0108 and expiration date of 19/08/2029.

  • Brand
    Medicrea International
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Compatibility

    Verify if your Universal Counter Torque (A22020500) is compatible with the Pass TULIP [Spinal] System nut driver (A22020220).

Where it went and when

Where it was distributed

Distributed in California and Florida.

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: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: 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: yesFL

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

States: California, Florida.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Nov 11, 201912. FDA classified it Class II: Feb 14, 202023. Published in FDA’s Enforcement Report: Feb 26, 202034. FDA terminated the recall: Oct 14, 2020420192020
  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-1234-2020 (November 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1234-2020 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