Musculoskeletal Transplant Foundation, Inc. recalls DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous…
Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.
Read the official notice →- Date
- 2023-11-29
- Country
- United States
- Brand
- Musculoskeletal Transplant Foundation
- Product
- DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of PA, TX, WA.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Musculoskeletal Transplant Foundation recalls
- 2024-02-21
USMusculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
FDA · DeviceMusculoskeletal Transplant Foundation, Inc.Product was distributed to Minnesota.Official notice →
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