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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93075

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

Open FDA event record

Event summary

Timeline bucket
September 20, 2023
Product types
Device
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
Cardinal Health 200, LLC

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

6 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 6

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

Z-0145-2024
Recall number
Z-0145-2024
Initiated
September 20, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Cardinal Health 200, LLC
Quantity
3,113,846 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Demonstrated recognition and compatibility issues with syringe infusion pumps.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Vendor change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Demonstrated recognition and compatibility issues with syringe infusion pumps.

Code information

Product Code: 1180100777; UDI/DI: 10192253034530 - each, 20192253034537 - box, 50192253034538 - case; Lot Numbers: 221201, 221202, 221203, 230201, 230202, 230203, 230204, 230205, 230601

Distribution pattern

US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.

device · product 2 of 6

Monoject" 6 mL Syringe Luer-Lock Tip Soft Pack

Z-0146-2024
Recall number
Z-0146-2024
Initiated
September 20, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Cardinal Health 200, LLC
Quantity
3,936,682 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Demonstrated recognition and compatibility issues with syringe infusion pumps.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Vendor change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Demonstrated recognition and compatibility issues with syringe infusion pumps.

Code information

Product Code: 1180600777; UDI/DI: 10192253034608 - each, 20192253034605 - box, 50192253034606 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206, 230207

Distribution pattern

US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.

device · product 3 of 6

Monoject" 12 mL Syringe Luer-Lock Tip Soft Pack

Z-0147-2024
Recall number
Z-0147-2024
Initiated
September 20, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Cardinal Health 200, LLC
Quantity
3,084,300 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Demonstrated recognition and compatibility issues with syringe infusion pumps.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Vendor change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Demonstrated recognition and compatibility issues with syringe infusion pumps.

Code information

Product Code: 1181200777T; UDI/DI: 10192253025811 - each, 20192253025818 - box, 50192253025819 - case; Lot Numbers: 221101, 221102, 221103, 221104

Distribution pattern

US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.

device · product 4 of 6

Monoject 20 mL Syringe Luer-Lock Tip Soft Pack

Z-0148-2024
Recall number
Z-0148-2024
Initiated
September 20, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Cardinal Health 200, LLC
Quantity
4,913,520 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Demonstrated recognition and compatibility issues with syringe infusion pumps.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Vendor change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Demonstrated recognition and compatibility issues with syringe infusion pumps.

Code information

Product Code: 1182000777; UDI/DI: 10192253034677 - each, 20192253034674 - box, 50192253034675 - case; Lot Numbers: 221201, 221202, 221203, 221204, 221205, 230201, 230202, 230203, 230204, 230205, 230206

Distribution pattern

US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.

device · product 5 of 6

Monoject" 35 mL Syringe Luer-Lock Tip Soft Pack

Z-0149-2024
Recall number
Z-0149-2024
Initiated
September 20, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Cardinal Health 200, LLC
Quantity
1,097,048 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Demonstrated recognition and compatibility issues with syringe infusion pumps.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Vendor change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Demonstrated recognition and compatibility issues with syringe infusion pumps.

Code information

Product Code: 1183500777; UDI/DI: 10192253034691 - each, 20192253034698 - box, 50192253034699 - case; Lot Numbers: 221201, 230201, 230601, 230602

Distribution pattern

US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.

device · product 6 of 6

Monoject" 60 mL Syringe Luer-Lock Tip Soft Pack

Z-0150-2024
Recall number
Z-0150-2024
Initiated
September 20, 2023
Classification
Class I
Status
Ongoing
Recalling firm
Cardinal Health 200, LLC
Quantity
457,200 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Demonstrated recognition and compatibility issues with syringe infusion pumps.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Vendor change control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Demonstrated recognition and compatibility issues with syringe infusion pumps.

Code information

Product Code: 1186000777T; UDI/DI: 10192253025835 - each, 20192253025832 - box, 50192253025833 - case; Lot Numbers: 221101, 230601

Distribution pattern

US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.