--- title: "Cerapedics, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Cerapedics, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/cerapedics-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Cerapedics, Inc. recall records **1** reported ongoing 2 records in this archive. Latest source date Dec 29, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Dec 29, 2025 FDA device enforcement ### [PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010](https://isitonrecall.com/recall/fda-device-z-1165-2026-pearmatrix-p-15-peptide-enhanced-bone-graft-bone-graft-1-0cc-ref-730-010/) Incorrect expiration date Class II Reported ongoing Distribution: US Nationwide distribution in the states of CA, CO, CT, FL, GA, ID, IL, KS, LA, MI, MN, MO, MT, NE, NJ, NV, NY, OH,OR, PA, TN, TX, WA, WY. [Official source for PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1165-2026%22) Apr 14, 2022 FDA device enforcement ### [putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY](https://isitonrecall.com/recall/fda-device-z-1056-2022-putty-i-factor-peptide-enhanced-bone-graft-1-0cc-syringe-ref-700-010-putty/) Patient chart label contains incorrect Part Number and volume amount. Class III Reported terminated Distribution: U.S. Nationwide distribution in the states of AL, AZ, CA, CT, DC, DE, ID, IN, KS, KY, MD, MI, MN, MO, NC, NV, NY, OH, PA, TX, VA, and WA. [Official source for putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1056-2022%22) ## Reasons in these listed records - Incorrect expiration date - Patient chart label contains incorrect Part Number and volume amount. These examples come from this result page and are not a ranking of every recall reason. ## Checking Cerapedics, Inc. ### Is there a recall on cerapedics, inc. right now? This archive contains 2 records, including 1 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Cerapedics, Inc.](https://isitonrecall.com/check/?q=Cerapedics%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)