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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93952

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 14, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Peter Lazic Gmbh

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile

Z-1287-2024
Recall number
Z-1287-2024
Initiated
July 14, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Peter Lazic Gmbh
Quantity
170 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Wrong product coloring. The paddle clips should be blank, but they are colored blue.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Wrong product coloring. The paddle clips should be blank, but they are colored blue.

Code information

Model Number: S.45.782; UDI/DI: 04250603734697; Serial Numbers: LX61400, LX61401, LX63366, LX63368, LX63369, LX63370, LX63371, LX63372, LX63373, LX63374, LX63375, LX65981, LX65982, LX65983, LX65984, LX66073, LX66074, LX66075, LX61372, LX61373, LX61374, LX61375, LX61376, LX61377, LX61378, LX61379, LX61380, LX61381, LX61382, LX61383, LX61384, LX61385, LX61386, LX61387, LX61388, LX61389, LX61389, LX61390, LX61391, LX61392, LX61393, LX61394, LX61395, LW50566, LW50567, LW50568, LX72845, LX72846, LX72847, LX72848, LX72849, LX72850, LX72851, LX72852, LX72853, LX72854;

Distribution pattern

US Nationwide distribution in the state of ME.

device · product 2 of 2

L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile

Z-1288-2024
Recall number
Z-1288-2024
Initiated
July 14, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Peter Lazic Gmbh
Quantity
51 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Wrong product coloring. The paddle clips should be blank, but they are colored blue.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Wrong product coloring. The paddle clips should be blank, but they are colored blue.

Code information

Model Number: 45.782; UDI/DI: 04250603733799; Serial Numbers: LX61385, LW36020, LW36021, LW36022, LW36023, LW36024, LW36025, LW36026, LW36027;

Distribution pattern

US Nationwide distribution in the state of ME.