Lower riskMedical device recall · FDA · Published April 7, 2025
Bio 1 Granules for Filling: Risk of Incorrect Product Amount
SCIENCE & BIO MATERIALS recalls Bio 1 Granules for Filling (REF:P822692243) due to potential underfilling. Check lot numbers 240781/UDI: 03760154000369 for affected items.
“Bio 1 Granules for Filling: Risk of Incorrect Product Amount.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52485-bio-1-granules-for-filling-risk-of-incorrect-product-amount. Based on FDA recall #Z-1718-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1718-2025%22&limit=1).
The FDA announced on April 7, 2025, that SCIENCE & BIO MATERIALS is recalling Bio 1 Granules for Filling ¿ 1 mm (2 cm¿) because vials may contain less product than specified. The agency issued recall number Z-1718-2025 for the Class II voluntary recall.
How to tell if you have it
Brand: SCIENCE & BIO MATERIALS
Product: Bio 1 Granules for Filling ¿ 1 mm (2 cm¿)
REF: P822692243
Material: BIOSORB (BTCP 95% minimum purity)
Lot #: 240781/UDI: 03760154000369
Quantity: 30 vials
The hazard
According to the FDA, vials of implant bone granules may contain less product than specified on labeling. The recall covers 30 vials distributed nationwide.
Context
GovInfoNow's records show SCIENCE & BIO MATERIALS has one other recall on record since 2021-10-07, specifically the ComposiTCP 30 Interference Screw recalled on that date for being a mislabeled product. Other recent recalls of similar products include Medtronic Bio-Medicus Adult Cannula Kit Recall (2026-05-25), Medline Medical Kits Recalled Due to Possible Bacillus Contamination (2026-06-11), and AVID Medical Haylard Basic Biopsy Tray Recall (2026-08-10).
How to tell if you have this one
Check for lot number 240781 and UDI code 03760154000369 on the vial. The product is labeled as Bio 1 Granules for Filling (1 mm, 2 cm).
Brand
SCIENCE & BIO MATERIALS
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for lot number 240781 and UDI code 03760154000369 on the vial.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
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 37 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1718-2025 (April 7, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1718-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 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.