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Lower risk Medical device recall · FDA · Published October 7, 2021

ComposiTCP 30 Interference Screw: Mislabeled Product Recall

SCIENCE & BIO MATERIALS recalls ComposiTCP 30 Interference screws with mislabeled product codes. Affected items have specific model and lot numbers. Consumers should check their purchases for the correct labeling.

🇺🇸 FDA recall #Z-1361-2022Medical deviceSCIENCE & BIO MATERIALS ›
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Recalling firmSCIENCE & BIO MATERIALSZi Du Monge · Lourdes, France
✎ GovInfoNow plain-language explainer

SCIENCE & BIO MATERIALS is recalling ComposiTCP 30 Interference screws that were mislabeled. This means the product may not match the intended specifications, which could lead to improper use or safety issues if the wrong screw is used in a project. Read more at govinfonow.com/recall/61711-compositcp-30-interference-screw-mislabeled-product-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/61711-compositcp-30-interference-screw-mislabeled-product-recall · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1361-2022

Cite this page

“ComposiTCP 30 Interference Screw: Mislabeled Product Recall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61711-compositcp-30-interference-screw-mislabeled-product-recall. Based on FDA recall #Z-1361-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1361-2022%22&limit=1).

The FDA announced on Oct. 7, 2021, that SCIENCE & BIO MATERIALS voluntarily recalled ComposiTCP 30 Interference screw D 7- L:25 mm due to mislabeling. The agency issued recall number Z-1361-2022 for the Class II device distributed nationwide.

How to tell if you have it

  • ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605
  • UPC 03760154006767
  • Lot #: 190491
  • Use before 01/01/2022

The hazard

The product was mislabeled, according to the FDA. The recall covers 72 units distributed nationwide in the U.S.

Context

GovInfoNow's records show SCIENCE & BIO MATERIALS has one other recall on record since April 7, 2025, involving Bio 1 Granules for Filling due to a risk of incorrect product amount. Other recent recalls of similar products include Synthes 2.4V TAP CORTEX SCREW Recall (Feb. 25, 2026), Tornier Perip Screw Recall (Dec. 19, 2025), and Smith & Nephew BIOSURE HA Screw Recall (Nov. 24, 2025).

How to tell if you have this one

Check for the product code 110004605 and lot number 190491 on the packaging. The screws were sold with a use-by date of January 1, 2022.

  • Brand
    SCIENCE & BIO MATERIALS
  • Product
    ComposiTCP 30 Interference screw D 7- L:25 mm, REF 110004605
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labeling

    Look for the product code 110004605 and lot number 190491 on the packaging to confirm if the screw is affected.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

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

Distributed nationwide.

Recall timeline

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

1. Firm started the recall: Oct 7, 202112. FDA classified it Class II: Jul 8, 202223. Published in FDA’s Enforcement Report: Jul 20, 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-1361-2022 (October 7, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1361-2022 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