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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 62747

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 03, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Medical Specialties Distributors, 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

1 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 1

Medstream 81" (206 cm) 20 Drop Standard bore Universal Administration Set with Y-Site, Sterile Manufactured for MSD (Medical Specialties Distributors LLC, Stoughton, MA. Product of China Product Number: MS721 Disposable Infusion set

Z-2179-2012
Recall number
Z-2179-2012
Initiated
August 03, 2012
Classification
Class II
Status
Terminated
Quantity
472 cases (50/case)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Devices leaking at the Y-site

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

Devices leaking at the Y-site

Code information

LOT NUMBER: 20111115

Distribution pattern

Nationwide Distribution