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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71569

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

Open FDA event record

Event summary

Timeline bucket
June 04, 2015
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Gardner Denver Thomas Inc

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

3 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 3

THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1240 Product Usage: medical aspirator

Z-2149-2015
Recall number
Z-2149-2015
Initiated
June 04, 2015
Classification
Class II
Status
Terminated
Recalling firm
Gardner Denver Thomas Inc
Quantity
160 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Vacuum pump may not perform to specification.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Vacuum pump may not perform to specification.

Code information

Serial Numbers 2639-2798

Distribution pattern

Internationally Distributed in the countries of :Mexico, Peru, El Salvador, Chile, Colombia, Vietnam, and Malaysia.

device · product 2 of 3

THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1242 Product Usage: medical aspirator

Z-2150-2015
Recall number
Z-2150-2015
Initiated
June 04, 2015
Classification
Class II
Status
Terminated
Recalling firm
Gardner Denver Thomas Inc
Quantity
370 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Vacuum pump may not perform to specification.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Vacuum pump may not perform to specification.

Code information

Serial numbers 3831-4200

Distribution pattern

Internationally Distributed in the countries of :Mexico, Peru, El Salvador, Chile, Colombia, Vietnam, and Malaysia.

device · product 3 of 3

THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1243 Product Usage: medical aspirator

Z-2151-2015
Recall number
Z-2151-2015
Initiated
June 04, 2015
Classification
Class II
Status
Terminated
Recalling firm
Gardner Denver Thomas Inc
Quantity
508 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Vacuum pump may not perform to specification.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Vacuum pump may not perform to specification.

Code information

Serial numbers 2122-2629

Distribution pattern

Internationally Distributed in the countries of :Mexico, Peru, El Salvador, Chile, Colombia, Vietnam, and Malaysia.