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Lower risk Medical device recall · FDA · Published January 26, 2024

In2Bones I.B.S 6.5-C Compression Screw Recall: Length Mix-Up Risk

In2Bones recalls I.B.S 6.5-C Compression screws (diam 6.5mm, lg 80mm) due to possible length mix-up with labeled 75mm screws. Affected units have batch number 2306008 and expire May 2028.

🇺🇸 FDA recall #Z-1320-2024Medical deviceIn2Bones ›
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Recalling firmIn2Bones, SAS28 Chemin du petit Bois · Ecully, France
✎ GovInfoNow plain-language explainer

In2Bones is recalling I.B.S 6.5-C Compression screws that may have incorrect lengths (80mm instead of 75mm) compared to their labels. This mix-up could lead to improper installation if used in medical applications. Read more at govinfonow.com/recall/56243-in2bones-i-b-s-6-5-c-compression-screw-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/56243-in2bones-i-b-s-6-5-c-compression-screw-recall · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1320-2024

Cite this page

“In2Bones I.B.S 6.5-C Compression Screw Recall: Length Mix-Up Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56243-in2bones-i-b-s-6-5-c-compression-screw-recall. Based on FDA recall #Z-1320-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1320-2024%22&limit=1).

In2Bones, SAS voluntarily recalled I.B.S. 6.5-C Compression screws (Part Number S65 ST180) following a batch mix-up that may result in incorrect screw lengths, the FDA said on Jan. 26, 2024.

How to tell if you have it

  • Brand: In2Bones
  • Product: I.B.S. 6.5-C Compression screw - diam 6.5mm lg 80mm
  • Part Number: S65 ST180
  • UDI/DI: 3760225710692
  • Batch Number: 2306008
  • Expiration Date: 31/MAY/2028
  • Quantity: 63 units

The hazard

The recall addresses a batch mix-up between I.B.S Compression screws diameter 6.5mm length 75mm and those with a length of 80mm. Consequently, the screws may have different lengths from those indicated on their labels.

Context

GovInfoNow's records show In2Bones, SAS has two other recalls on file since July 13, 2017, including a Feb. 9, 2021 recall for Shannon Percutaneous Burr breakage and a July 13, 2017 recall for Non-Locking Screws fracture risk. Other recent recalls of similar products include Synthes 2.4V TAP CORTEX SCREW (Feb. 25, 2026), Tornier Perip Screw (Dec. 19, 2025), and Smith & Nephew BIOSURE HA Screw (Nov. 24, 2025).

How to tell if you have this one

Check for the part number S65 ST180 and batch number 2306008 on the screw packaging. The screws expire by May 2028 and are labeled as 80mm in length.

  • Brand
    In2Bones
  • Category
    Medical device
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    US Nationwide distribution in the state of Tennessee.
Recall numberProduct, codes & lotsQuantity
Z-1319-2024I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175; UDI/DI 3760225710685, Batch Number 2306007, exp. 31/MAY/202859 units
Z-1320-2024I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180; UDI/DI 3760225710692, Batch Number 2306008, exp. 31/MAY/202863 units
Based on the official FDA remedy

What to do — step by step

  1. Check Screw Length

    Verify the actual length of the screw against the label (should be 80mm, not 75mm).

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 in the state of Tennessee.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

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

1. Firm started the recall: Jan 26, 202412. FDA classified it Class II: Mar 20, 202423. Published in FDA’s Enforcement Report: Mar 27, 202432024
  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-1320-2024 (January 26, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1320-2024 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