Lower riskMedical device recall · FDA · Published February 2, 2022
Ace Surgical NuOss Collagen Block Recall: Suboptimal Bone Repair Risk
Ace Surgical recalls NuOss Collagen Blocks (8mm x 9mm x 9mm) for possible suboptimal bone repair in dental procedures. Affected items have specific catalog and lot numbers.
NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for oral wounds) rather than NuOss Collagen Block, may result in suboptimal bone repair
Take action
Contact the company
📍Recalling firmAce Surgical Supply Co., Inc.1034 Pearl St · Brockton, MA 02301-5411
“Ace Surgical NuOss Collagen Block Recall: Suboptimal Bone Repair Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61187-ace-surgical-nuoss-collagen-block-recall-suboptimal-bone-repair-risk. Based on FDA recall #Z-0823-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0823-2022%22&limit=1).
The FDA announced on Feb. 2, 2022, that Ace Surgical Supply Co., Inc. recalled NuOss Collagen Block Size 8mm x 9mm x 9mm due to packaging errors. The hazard involves receiving Collatene Fibrillar Collagen instead of the intended product, which may result in suboptimal bone repair.
How to tell if you have it
Brand: Ace Surgical Supply
Product: NuOss Collagen Block Size 8mm x 9mm x 9mm
Catalog Number: 5099250
Lot Number: BMBU21A1
Expiration Date: 2024-03-31
UDI: 00614950007264
The hazard
NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen for oral wounds rather than NuOss Collagen Block. This error may result in suboptimal bone repair.
Context
GovInfoNow's records show Ace Surgical Supply Co., Inc. has two other recalls on record since Oct. 24, 2017. Other recent recalls of similar products include Straumann GM Helix Dental Implant Recall (July 13, 2026), F & A Foundation Reign Medical Clench Staple System Recall (July 15, 2026), and Straumann Bone Level Tapered Implant May Be Wrong Length - Recall (July 16, 2026).
How to tell if you have this one
Check for catalog number 5099250 and lot number BMBU21A1 with expiration date 2024-03-31. The product is used in dental procedures for filling periodontal and maxillofacial defects.
Brand
Ace Surgical Supply
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Verify Product Details
Check the catalog number (5099250) and lot number (BMBU21A1) on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 4 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution in the states of GA, NY, VA, WI and the countries of France, Germany.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Georgia, New York, Virginia, Wisconsin.
Recall timeline
FDA published this recall 56 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 recall indicates a potential risk of suboptimal bone repair, but the product is not unsafe in normal use. Dentists should verify the correct product before use.
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-0823-2022 (February 2, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0823-2022 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.