PlainRecalls
FDA Devices Moderate Class II Ongoing

OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01.

Reported: January 22, 2025 Initiated: November 27, 2024 #Z-0919-2025

Product Description

OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01.

Reason for Recall

Hydration issue resulting in the product being less cohesive and moldable than intended due to an issue with the polymer.

Details

Units Affected
145
Distribution
US Nationwide distribution in the states of AL, CA, MD. MN, MS, NC, NV, OH, OK, TX.
Location
Irvine, CA

Frequently Asked Questions

What product was recalled?
OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01.. Recalled by IsoTis OrthoBiologics, Inc.. Units affected: 145.
Why was this product recalled?
Hydration issue resulting in the product being less cohesive and moldable than intended due to an issue with the polymer.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 22, 2025. Severity: Moderate. Recall number: Z-0919-2025.