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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 90707

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

Open FDA event record

Event summary

Timeline bucket
August 01, 2022
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
CAREFUSION

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

9 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 9

BD MaxGuard Extension Set with 4-way stopcock, REF: M4058

Z-1752-2022
Recall number
Z-1752-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
46,900

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403235788, Lots: 22019324, 22019323, 22019322

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 2 of 9

BD MaxGuard Extension Set, REF: ME1069

Z-1753-2022
Recall number
Z-1753-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
3,500

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403236037, Lots: 22019062

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 3 of 9

BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS106

Z-1754-2022
Recall number
Z-1754-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
54,050

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403236358, Lots: 22019311, 22019312, 22019313, 22019314

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 4 of 9

BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141

Z-1755-2022
Recall number
Z-1755-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
37,550

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403236471, Lots: 22029167, 22029168, 22029169

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 5 of 9

BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold and removable 4-way stopcock, REF: MX4436

Z-1756-2022
Recall number
Z-1756-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
19,925

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403237478, Lots: 22019074, 22019431, 22019075, 22019076

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 6 of 9

BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059

Z-1757-2022
Recall number
Z-1757-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
17,250

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403237584, Lots: 22029431, 22029432

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 7 of 9

BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166

Z-1758-2022
Recall number
Z-1758-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
600

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403237652, Lots: 22029648

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 8 of 9

BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171

Z-1759-2022
Recall number
Z-1759-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
100

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403237669, Lots: 22029674

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN

device · product 9 of 9

BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433

Z-1760-2022
Recall number
Z-1760-2022
Initiated
August 01, 2022
Classification
Class II
Status
Ongoing
Recalling firm
CAREFUSION
Quantity
9,900

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Error in labeling

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.

Code information

UDI-DI: 10885403237782, Lots: 22019085

Distribution pattern

US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN