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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81837

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

Open FDA event record

Event summary

Timeline bucket
February 02, 2018
Product types
Device
Classifications
Class II
Statuses
Completed
Recalling firm wording
Shippert Medical Technologies

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

7 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 7

Tissu-Trans FILTRON 100, Catalog 3-TT-FILTRON 100, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Z-1330-2019
Recall number
Z-1330-2019
Initiated
February 02, 2018
Classification
Class II
Status
Completed
Quantity
6,553 units were distributed for all catalog numbers

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

Code information

Lot numbers 61472, 61601, 61816, 61817, 61818, 61819, 61878, 61736, 61801, 61948, 62050, and 62139.

Distribution pattern

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

device · product 2 of 7

Tissu-Trans FILTRON 250, Catalog 3-TT-FILTRON 250, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Z-1331-2019
Recall number
Z-1331-2019
Initiated
February 02, 2018
Classification
Class II
Status
Completed
Quantity
6,553 units were distributed for all catalog numbers

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

Code information

Lot numbers 61507, 61578, 61682, 61689, 61849, 61879, 62011, 62088, and 62108

Distribution pattern

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

device · product 3 of 7

Tissu-Trans FILTRON 500, Catalog 3-TT-FILTRON 500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Z-1332-2019
Recall number
Z-1332-2019
Initiated
February 02, 2018
Classification
Class II
Status
Completed
Quantity
6,553 units were distributed for all catalog numbers

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

Code information

Lot numbers 61508, 61636, 61683, 61753, 61804, 61812, 61813, 61814, 61815, 61862, 61917, 61949, 61991, 62052, 62089, 62134, and 62156

Distribution pattern

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

device · product 4 of 7

Tissu-Trans FILTRON 1000, Catalog 3-TT-FILTRON 1000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Z-1333-2019
Recall number
Z-1333-2019
Initiated
February 02, 2018
Classification
Class II
Status
Completed
Quantity
6,553 units were distributed for all catalog numbers

App-derived interpretation

No assignment exists because the official recall reason is blank.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Unavailable

Code information

61627, 61687, 61839, 61920, 62051, and 62087

Distribution pattern

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

device · product 5 of 7

Tissu-Trans FILTRON 2000, Catalog 3-TT-FILTRON 2000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Z-1334-2019
Recall number
Z-1334-2019
Initiated
February 02, 2018
Classification
Class II
Status
Completed
Quantity
6,553 units were distributed for all catalog numbers

App-derived interpretation

No assignment exists because the official recall reason is blank.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Unavailable

Code information

61688, 61759, 61846, 61847, and 61848

Distribution pattern

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

device · product 6 of 7

Tissu-Trans MEGA 1500, Catalog 3-TT-MEGA 1500, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Z-1335-2019
Recall number
Z-1335-2019
Initiated
February 02, 2018
Classification
Class II
Status
Completed
Quantity
6,553 units were distributed for all catalog numbers

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

Code information

61471, 61625, 61754, 61840, 61945, 61950, 62135, 62137, and 62157

Distribution pattern

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

device · product 7 of 7

Tissu-Trans Syringe Fill 360, Catalog 3-TT-SFILL 360, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.

Z-1336-2019
Recall number
Z-1336-2019
Initiated
February 02, 2018
Classification
Class II
Status
Completed
Quantity
6,553 units were distributed for all catalog numbers

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.

Code information

61656

Distribution pattern

Distribution was nationwide, including PR. There was government/military distribution. Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,