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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98659

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

Open FDA event record

Event summary

Timeline bucket
March 11, 2026
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Windstone Medical Packaging, 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

3 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 3

Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14433

Z-1919-2026
Recall number
Z-1919-2026
Initiated
March 11, 2026
Classification
Class II
Status
Ongoing
Quantity
475 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).

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

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).

Code information

UDI-DI: B098AMS144330; Lot Numbers: 204612 206723 210211 213641 216064 222060 224073 225012 236012 236910

Distribution pattern

US Nationwide distribution in the states of GA, OR, TN, and WA.

device · product 2 of 3

Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994

Z-1920-2026
Recall number
Z-1920-2026
Initiated
March 11, 2026
Classification
Class II
Status
Ongoing
Quantity
380 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).

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

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).

Code information

UDI-DI: B098AMS149940; Lot Numbers: 220039 221423 224226 224793 225009

Distribution pattern

US Nationwide distribution in the states of GA, OR, TN, and WA.

device · product 3 of 3

Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994A

Z-1921-2026
Recall number
Z-1921-2026
Initiated
March 11, 2026
Classification
Class II
Status
Ongoing
Quantity
520 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).

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

The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).

Code information

UDI-DI: B098AMS14994A0; Lot Numbers: 224792 228566 230105 230853 234209

Distribution pattern

US Nationwide distribution in the states of GA, OR, TN, and WA.

Field note

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