Recall Z-2365-2015— Cadence Inc.
Class II · Terminated
Class II FDA medical device recall by Cadence Inc., initiated 2015-07-09, terminated 2016-07-29. FDA's recall record names no specific 510(k) clearance for this event. Product: Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209. Reason: Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel..
- Recalling firm
- Cadence Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-07-09
- Terminated
- 2016-07-29
- Firm location
- Cranston, RI, United States
Product description
Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209
Reason for recall
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
Data sourced from openFDA. This site is unofficial and independent of the FDA.