Recall Z-1446-2013— Leica Microsystems, Inc.
Class II · Terminated
Class II FDA medical device recall by Leica Microsystems, Inc., initiated 2013-04-04, terminated 2017-07-21. FDA's recall record names no specific 510(k) clearance for this event. Product: LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848; 14060546846; 14060546845; 14060546933; 14060546932; 14060546852; 14060546850; 14060546847. The intended use of this device is for storage of specimens/tissues during processing.. Reason: An LPC Fine Mesh Cassette failed to stay closed during processing operations..
- Recalling firm
- Leica Microsystems, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-04-04
- Terminated
- 2017-07-21
- Firm location
- Buffalo Grove, IL, United States
Product description
LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848; 14060546846; 14060546845; 14060546933; 14060546932; 14060546852; 14060546850; 14060546847. The intended use of this device is for storage of specimens/tissues during processing.
Reason for recall
An LPC Fine Mesh Cassette failed to stay closed during processing operations.
Data sourced from openFDA. This site is unofficial and independent of the FDA.