Recall Z-2124-2014— DeRoyal Industries Inc
Class II · Terminated
Class II FDA medical device recall by DeRoyal Industries Inc, initiated 2014-06-04, terminated 2015-05-05. FDA's recall record names no specific 510(k) clearance for this event. Product: DeRoyal KNEE ARTHROSCOPY PACK, REF 89-6192.04, 1 Per Pack, Distributed by: DeRoyal Industries, Inc.; Manufacturer: DeRoyal Industries, Inc.. Reason: The firm distributed surgical kits which contained Irrigation Sets which were subsequently recalled by Hospira..
- Recalling firm
- DeRoyal Industries Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-06-04
- Terminated
- 2015-05-05
- Firm location
- Powell, TN, United States
Product description
DeRoyal KNEE ARTHROSCOPY PACK, REF 89-6192.04, 1 Per Pack, Distributed by: DeRoyal Industries, Inc.; Manufacturer: DeRoyal Industries, Inc.
Reason for recall
The firm distributed surgical kits which contained Irrigation Sets which were subsequently recalled by Hospira.
Data sourced from openFDA. This site is unofficial and independent of the FDA.