PlainRecalls
FDA Devices Moderate Class II Ongoing

Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A

Reported: August 28, 2024 Initiated: July 25, 2024 #Z-2688-2024

Product Description

Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A

Reason for Recall

At least two units have been found to be missing a weld.

Details

Units Affected
207 units
Distribution
US Nationwide distribution.
Location
Woburn, MA

Frequently Asked Questions

What product was recalled?
Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A. Recalled by Intrinsic Therapeutics, Inc.. Units affected: 207 units.
Why was this product recalled?
At least two units have been found to be missing a weld.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 28, 2024. Severity: Moderate. Recall number: Z-2688-2024.