Depuy Mitek, a Johnson & Johnson Co. Recalls

FDA
3
Total Recalls
1
Agencies
May 2006
First Recall
Jun 2006
Latest Recall
Sort: Newest first Highest severity

Showing 1-3 of 3 recalls

FDA

Depuy Mitek Bioknotless Anchor with Ethibond Suture Ref No. 212728

The inserter shafts bend, as they were manufactured with a different stainless steel than specified.

Depuy Mitek notified consignees by letter dated 2/17/06 to request accounts return devices.
FDA

Depuy Mitek Fastin RC Anchor with Panacryl (2) strands Size 2 Panacryl Poly ***braided absorbable suture Reference Number: 222740

The device may contain one strand of suture instead of two strands

DePuy Mitek initiated the recall to domestic accounts by letter on 10/27/05 and to J & J Affiliates by email.
FDA

DePuy Mitek Straightshot Ligament Graft Passer/Protector, 11.5 mm Catalog Number : 232220

Mislabeled: The kit contained the incorrect Ligament Passer. The package contained a 9.5 mm instead of the labeled 11.5mm ligament passer

DePuy Mitek notified the accounts by US Mail on 8/09/05. Accounts were requested to return product.