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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79031

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

Open FDA event record

Event summary

Timeline bucket
August 02, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Haemonetics Corporation

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

Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for Use: The Haemonetics Cell Saver 5/5+ System and its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.

Z-0778-2019
Recall number
Z-0778-2019
Initiated
August 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Haemonetics Corporation
Quantity
11,208 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Haemonetics has received isolated reports that in some cases the 70ml centrifuge bowl may leak during cell salvage processing.

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

Haemonetics has received isolated reports that in some cases the 70ml centrifuge bowl may leak during cell salvage processing.

Code information

Catalog number: 0291A-00, 0291E-00

Distribution pattern

US Nationwide Distribution to states of: AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, LA, MA, MD, ME, MN, MO, NC, NE, NH, NJ, NY, OH, OR, PA, SC, TN, TX, VA, WA, and WI.

device · product 2 of 2

Cell Saver Elite Processing Kit, 70 ml, Product ID: CSE-P-70 Indications for Use: The Haemonetics Cell Saver 5/5+ System and its related accessory components are intended to be used for the recovery and processing of blood shed during or subsequent to an operation or as a result of trauma.

Z-0779-2019
Recall number
Z-0779-2019
Initiated
August 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Haemonetics Corporation
Quantity
4576 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Haemonetics has received isolated reports that in some cases the 70ml centrifuge bowl may leak during cell salvage processing.

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

Haemonetics has received isolated reports that in some cases the 70ml centrifuge bowl may leak during cell salvage processing.

Code information

Catalog number: CSE-P-70

Distribution pattern

US Nationwide Distribution to states of: AL, AZ, CA, CO, CT, FL, GA, ID, IL, IN, LA, MA, MD, ME, MN, MO, NC, NE, NH, NJ, NY, OH, OR, PA, SC, TN, TX, VA, WA, and WI.