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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94823

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

Open FDA event record

Event summary

Timeline bucket
June 17, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
B. Braun Medical, 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

29 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 29

OUTLOOK IV SET 15DROP W/2 CARESITE-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication. Model/Catalog Number: 354212

Z-2376-2024
Recall number
Z-2376-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
236208 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964293832. All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 2 of 29

OUTLOOK IV SET 15DROP W/3 CARESITE-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication. Model/Catalog Number: 354213

Z-2377-2024
Recall number
Z-2377-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
88968 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964182211; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 3 of 29

Infusomat UNIV.15DROP PUMP SET W/3 SAFELINE LL-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362032

Z-2378-2024
Recall number
Z-2378-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
1 unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964182556; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 4 of 29

Infusomat UNIV. 15 DR PUMP SET, 1.2 FIL, 2 CRSITE-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication. Model/Catalog Number: 362033

Z-2379-2024
Recall number
Z-2379-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
47370 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964837821; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 5 of 29

Infusomat 60DROP METRISET PUMP SET, 3 SAFELINE-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362034

Z-2380-2024
Recall number
Z-2380-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
280 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964182570; All Lots Distributed After 10AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 6 of 29

Infusomat UNIV. 15 DROP PUMP SET W/ 0.2 FILTER- Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362050

Z-2381-2024
Recall number
Z-2381-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
3624 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964182655; All Lots Distributed After 08AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 7 of 29

Infusomat SPACE PUMP SET 15 DROP W/2 SAFEDAY-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362420

Z-2382-2024
Recall number
Z-2382-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
431999 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046955592715; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 8 of 29

Infusomat UNIV. 15 DROP PUMP SET W/ 3 ULTRASITE LL-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362431

Z-2383-2024
Recall number
Z-2383-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
1152 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294013; All Lots Distributed After 02AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 9 of 29

Infusomat SPACE PUMP IV SET , 120 IN.- Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 362432

Z-2384-2024
Recall number
Z-2384-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
2160 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964182679; All Lots Distributed After 02AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 10 of 29

Infusomat 60 DROP METRISET PUMP SET,3 SFLINE ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363010

Z-2385-2024
Recall number
Z-2385-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
100 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294174; All Lots Distributed After 05SEP2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 11 of 29

Infusomat UNIV. 15 DROP PUMP SET W/3 SAFELINE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363030

Z-2386-2024
Recall number
Z-2386-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
37776 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294259; All Lots Distributed After 02AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 12 of 29

Infusomat SPACE PUMP IV SET, 2 CARESITES, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363420

Z-2387-2024
Recall number
Z-2387-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
68205 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294594; All Lots Distributed After 02AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 13 of 29

Infusomat UNIV. 15 DROP PUMP SET, 2 CARESITE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363421

Z-2388-2024
Recall number
Z-2388-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
1325700

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294617; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 14 of 29

Infusomat 60DROP METRISET PUMP, 3 CARESITES, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363422

Z-2389-2024
Recall number
Z-2389-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
7360 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294631; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 15 of 29

Infusomat UNIV. 60 DROP PUMP SET, 2 CARESITES, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363423

Z-2390-2024
Recall number
Z-2390-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
22560 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294655; All Lots Distributed After 04AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 16 of 29

Infusomat UNIV. 15 DR PUMP SET, 1.2FIL, 2CRSTE ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363424

Z-2391-2024
Recall number
Z-2391-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
32752 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964837906; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 17 of 29

Infusomat UNIV. 15 DROP PUMP SET, 3 CARESITE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363430

Z-2392-2024
Recall number
Z-2392-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
2085606 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294679; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 18 of 29

Infusomat UNIV. 15 DROP PUMP SET, 3 CARESITE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363433

Z-2393-2024
Recall number
Z-2393-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
42028 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964837920; All Lots Distributed After 03AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 19 of 29

Infusomat SPACE PUMP IV SET 15D, 110 IN. -Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 480254

Z-2394-2024
Recall number
Z-2394-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
109464 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046955324798; All Lots Distributed After 02AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 20 of 29

Infusomat SPACE PUMP IV SET, 127 IN.-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 480255

Z-2395-2024
Recall number
Z-2395-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
1872 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046955324804; All Lots Distributed After 06SEP2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 21 of 29

Infusomat SPACE PUMP IV SET 15D, 90 IN. Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number 480263

Z-2396-2024
Recall number
Z-2396-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
13464 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046955693931; All Lots Distributed After 25SEP2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 22 of 29

Infusomat UNIV. 15 DROP PUMP SET W 3 CARESITE L.L. Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 490100

Z-2397-2024
Recall number
Z-2397-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
6843513 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964186080; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 23 of 29

Infusomat 60 DROP METRISET PUMP SET, 3 CARESITES Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 490101

Z-2398-2024
Recall number
Z-2398-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
33065 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964186103; All Lots Distributed After 01AUG2023

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 24 of 29

Infusomat UNIV. 15 DROP PUMP SET W/2 CARESITE CV- Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number 490102

Z-2399-2024
Recall number
Z-2399-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
5672116 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964186127; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 25 of 29

Infusomat SPACE PUMP IV SET W/2 CARESITE, CKVLV -Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 490103

Z-2400-2024
Recall number
Z-2400-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
643608 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964302107; All Lots Distributed After 01AUG2023

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 26 of 29

Infusomat UNIV 60 DROP PUMP SET, W/2 CARESITE INJ. -Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number : 490104

Z-2401-2024
Recall number
Z-2401-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
59811 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964186141; All Lots Distributed After 01AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 27 of 29

Outlook OUTLOOK PUMP SET,3 CARESITE LADS,115 IN. Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 490361

Z-2402-2024
Recall number
Z-2402-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
9504 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964642623; All Lots Distributed After 03AUG2023

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 28 of 29

Infusomat UNIV. 15 DROP PUMP SET, 3 ULTRASITE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 363230

Z-2403-2024
Recall number
Z-2403-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
158904 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046964294495; All Lots Distributed After 01AUG2023

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.

device · product 29 of 29

OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/ Catalog Number: 490564

Z-2404-2024
Recall number
Z-2404-2024
Initiated
June 17, 2024
Classification
Class II
Status
Ongoing
Recalling firm
B. Braun Medical, Inc.
Quantity
2352 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

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

Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

Code information

UDI-DI 04046955275588; All Lots Distributed After 22AUG2023.

Distribution pattern

Worldwide distribution - US Nationwide and the country of Canada.