RecallRadar

FDA Device recall Z-1446-2013

LPC Fine Mesh Cassette for the Leica LPC Printer

On 2013-06-12 the FDA classified a Class II recall of LPC Fine Mesh Cassette for the Leica LPC Printer by Leica Microsystems, citing an LPC Fine Mesh Cassette failed to stay closed during processing operations.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1446-2013
ClassificationClass II
Statusterminated
Initiated2013-04-04
Published2013-06-12
Last updated2026-09-13 11:53 UTC
CompanyLeica Microsystems
DistributionUS

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.

Identifiers

code_info
1) Part No.: 14060546848; Batch No.s: 8280-10309, 82801-0310; 2) Part No.: 14060546846; Batch No.s: 1034710114;…1) Part No.: 14060546848; Batch No.s: 8280-10309, 82801-0310; 2) Part No.: 14060546846; Batch No.s: 1034710114; 3) Part No.: 14060546845; Batch No.s: 1021420914; 4) Part No.: 14060546933; Batch No.s: 82801-0217; 5) Part No.: 14060546932; Batch No.s: 1030730112, 1101110204; 6) Part No.: 14060546852; Batch No.s: 1101910322; 7) Part No.: 14060546850; Batch No.s: 1034710204, 1034710328, 1113910803; 8) Part No.: 14060546847; Batch No.s: 913920827

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1446-2013%22

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