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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 63959

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

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Event summary

Timeline bucket
December 20, 2012
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Medisystems a NX Stage Company

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

Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Code: BH-2035PE Product Usage: Medisystems Buttonhole Needle Sets are indicated for use as an access device for dialysis and pheresis procedures using a constant site orbuttonhole method of needle insertion.

Z-0714-2013
Recall number
Z-0714-2013
Initiated
December 20, 2012
Classification
Class II
Status
Terminated
Quantity
26 casesx 250 needles (6500needles)

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeled

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1" instead of 15 Ga x 3/5".

Code information

Lot: 120719F4

Distribution pattern

US Nationwide Distribution in the states of NY, PA and TN.

device · product 2 of 2

Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Code: D9-2007MGLB Product Usage: Medisystems AVF with MasterGuard anti-stick needle protector is indicated for use as a vascular access device in hemodialysis or other extracorporeal procedures. It is intended for use in conjunction with a blood tubing set equipped with a standard medical male luer-locking connector

Z-0715-2013
Recall number
Z-0715-2013
Initiated
December 20, 2012
Classification
Class II
Status
Terminated
Quantity
16 cases (15 cs x 250 ea) 4,000 needles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeled

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling mix-ups

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Single needle packs in each case ( 10 needles per case) are mislabeled on the pouch as 15 Gauge needles instead of 17 Gauge

Code information

Lot: Number: 110914F8

Distribution pattern

US Nationwide Distribution in the states of NY, PA and TN.