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FDA Medical Device Recalls (openFDA)

Cerapedics, Inc.: PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010

Recall number
Z-1165-2026
Recalling firm
Cerapedics, Inc.
Product
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Status
Open, Classified
Initiated
2025-12-29
Posted
2026-01-23
Terminated
not on file
Reason
Incorrect expiration date
Root cause
Labeling Change Control
Action
On December 29, 2025, Cerapedics issues a "Urgent: Medical Device Recall" notification to affected consignees via Email. Cerapedics asked consignees to take the following actions: 1. Please immediately examine your inventory and return any remaining units of PearlMatrix 1.0cc, lot 7014819. " RMA will be issued for this return and a shipping label. 2. Please acknowledge receipt of this letter by responding to this email or call toll-free at 1-866-360-5612. 3. If you have further distributed this product, please identify your customers, and notify them at once of this product recall. You may provide a copy of this recall notification letter to your customer.
Quantity
237 units
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.
Lot, serial or model codes
Lot: 7014819/UDI: (01)00850001680196
510(k) numbers
not on file
PMA numbers
["P240001"]
Product code
NOX
Firm FEI
3007155473
Firm city
Westminster
Firm state
CO
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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