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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82552

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

Open FDA event record

Event summary

Timeline bucket
April 01, 2019
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Teleflex Medical

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

5 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 5

RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0

Z-1682-2019
Recall number
Z-1682-2019
Initiated
April 01, 2019
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
1787 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

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

The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

Code information

Lot Numbers: 14151, 14161, 14171, 14211, 14231, 14271, 14281, 14321, 14441, 14461, 14501, 14511, 15031, 15051, 15091, 15101, 15251, 15271, 15411, 16051, 16071, 16101, 16161, 16171, 16201, 16231, 16271, 16291, 16301, 16311, 16361, 16381, 16401, 16421, 16431, 16451, 16481, 16501, 16511, 17021, 17031, 17051, 17071, 17091, 17111, 17121, 17161, 17181, 17191, 17201, 17251, 17261, 17271, 17281, 17351, 17371, 17461, 18021, 18031, 18061, 18101, 18121, 18161, 18201, 18351, 18361, 18401

Distribution pattern

Nationwide

device · product 2 of 5

RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0

Z-1683-2019
Recall number
Z-1683-2019
Initiated
April 01, 2019
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
5995 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

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

The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

Code information

Lot Numbers: 14151, 14161, 14171, 14201, 14211, 14231, 14261, 14271, 14291, 14451, 14461, 14491, 14511, 15041, 15081, 15091, 15101, 15131, 15161, 15201, 15211, 15221, 15241, 15251, 15361, 15381, 15391, 15411, 15431, 15441, 15461, 15491, 15501, 16041, 16051, 16061, 16081, 16091, 16111, 16121, 16141, 16161, 16171, 16191, 16201, 16221, 16231, 16241, 16251, 16261, 16281, 16291, 16301, 16351, 16361, 16371, 16381, 16391, 16401, 16421, 16431, 16441, 16451, 16471, 16481, 16501, 16511, 17021, 17041, 17051, 17061, 17071, 17081, 17091, 17101, 17121, 17131, 17161, 17171, 17181, 17191, 17201, 17211, 17231, 17271, 17281, 17301, 17311, 17361, 17371, 17391, 17421, 17431, 17441, 17451, 17461, 17471, 17481, 17491, 17501, 17511, 18021, 18031, 18041, 18051, 18061, 18071, 18081, 18091, 18101, 18111, 18121, 18131, 18141, 18151, 18171, 18191, 18201, 18231, 18241, 18271, 18351, 18361, 18381, 18401, 18421, 18431, 18441, 14141, 14161, 14171, 14201, 14211, 14231, 14261, 14271, 14281, 14291, 14301, 14311, 14361, 14431, 14441, 14461, 14471, 14481, 14501, 14511, 15041, 15051, 15071, 15081, 15091, 15111, 15121, 15161, 15191, 15211, 15231, 15251, 15311, 15361, 15371

Distribution pattern

Nationwide

device · product 3 of 5

RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0

Z-1684-2019
Recall number
Z-1684-2019
Initiated
April 01, 2019
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
4312 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

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

The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

Code information

Lot Numbers: 15411, 15421, 15431, 15441, 15451, 15461, 15471, 15501, 16031, 16061, 16081, 16091, 16101, 16131, 16151, 16161, 16171, 16181, 16191, 16201, 16221, 16231, 16241, 16251, 16261, 16281, 16291, 16301, 16311, 16351, 16361, 16371, 16381, 16391, 16421, 16431, 16441, 16451, 16461, 16471, 16481, 16501, 17021, 17031, 17041, 17051, 17061, 17081, 17091, 17101, 17111, 17121, 17131, 17161, 17171, 17181, 17191, 17201, 17221, 17231, 17251, 17261, 17271, 17281, 17291, 17301, 17361, 17381, 17411, 17421, 17431, 17441, 17451, 17461, 17471, 17481, 17491, 17501, 18021, 18031, 18041, 18051, 18061, 18071, 18091, 18101, 18111, 18121, 18131, 18141, 18151, 18161, 18171, 18201, 18221, 18231, 18241, 18251, 18281, 18301, 18311, 18381, 18401, 18411, 18421, 18431, 18441

Distribution pattern

Nationwide

device · product 4 of 5

RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0

Z-1685-2019
Recall number
Z-1685-2019
Initiated
April 01, 2019
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
4312 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

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

The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

Code information

Lot Numbers: 14161, 14171, 14201, 14211, 14231, 14261, 14301, 14311, 14361, 14431, 14481, 14491, 15041, 15051, 15081, 15091, 15121, 15131, 15161, 15171, 15201, 15221, 15241, 15261, 15371, 15411, 15421, 15501, 16031, 16071, 16111, 16151, 16161, 16181, 16201, 16221, 16241, 16251, 16271, 16281, 16291, 16301, 16351, 16361, 16371, 16381, 16391, 16401, 16421, 16441, 16461, 16471, 16481, 17061, 17071, 17161, 17191, 17211, 17221, 17251, 17271, 17291, 17301, 17311, 17381, 17391, 17411, 17471, 17481, 17511, 18021, 18081, 18091, 18151, 18161, 18211, 18241, 18291, 18381, 18411, 18421, 18431, 18441

Distribution pattern

Nationwide

device · product 5 of 5

RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0

Z-1686-2019
Recall number
Z-1686-2019
Initiated
April 01, 2019
Classification
Class II
Status
Terminated
Recalling firm
Teleflex Medical
Quantity
2325 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

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

The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

Code information

Lot Numbers: 14151, 14161, 14201, 14281, 14301, 14321, 14431, 14491, 14511, 15041, 15371, 15441, 16071, 16131, 16191, 16221, 16241, 16271, 16311, 16371, 16391, 16441, 16451, 16481, 16491, 17091, 17121, 17181, 17211, 17241, 17281, 17351, 17381, 17451, 17471, 17491, 18181, 18301, 18411

Distribution pattern

Nationwide

Field note

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