Exact FDA event identifier

Event 70974

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

Open FDA event record

Event summary

Timeline bucket: February 09, 2015
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: MRP, LLC dba AMUSA

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

T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush syringe.

Z-1808-2015

Recall number: Z-1808-2015
Initiated: February 09, 2015
Classification: Class II
Status: Terminated
Recalling firm: MRP, LLC dba AMUSA
Quantity: 1,080 units (3 cases)

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

Incorrect labeling

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

Incorrect labeling of the expiration date

Code information

KH04090

Distribution pattern

US distribution to CA only.