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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71543

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

Open FDA event record

Event summary

Timeline bucket
June 03, 2015
Product types
Device
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Elite Biomedical Solutions LLC

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

Alaris Medley LVP Frame Membrane. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.

Z-2371-2015
Recall number
Z-2371-2015
Initiated
June 03, 2015
Classification
Class I
Status
Terminated
Quantity
609 pieces

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.

Code information

P/N TC10006587 and 10013801 Lot Numbers 022015502 and 0421151000.

Distribution pattern

Nationwide Distribution in the states of AZ, CA, GA, IL, IN, KS, KY, MA, MD, MN, MO, MS, NC, NY, OH, PA, SC, TN, TX, VA & WI.

device · product 2 of 2

Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.

Z-2372-2015
Recall number
Z-2372-2015
Initiated
June 03, 2015
Classification
Class I
Status
Terminated
Quantity
346 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.

Code information

P/N 49000204 Lot #'s 031815100, 032415100, 04061545 and 043015215

Distribution pattern

Nationwide Distribution in the states of AZ, CA, GA, IL, IN, KS, KY, MA, MD, MN, MO, MS, NC, NY, OH, PA, SC, TN, TX, VA & WI.