Urgent site urgencyFDA Class I

MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit SKU CDS984556N

The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could result in drug ineffectiveness.

Agency: FDA Device
Recall date: Jun 8, 2026
Status: Ongoing
Company: Medline Industries, LP

1. What product was recalled?

MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit SKU CDS984556N

Quantity: 52 kits

Code or lot text: UDI/DI 10198459266621 (each) 40198459266622 (case), Lot Numbers: 26EDA285, 26DDA718, 26BDB740, 26ADB079, 26ADA161, 25KDB472, 25GDA213.

LOT: 25GDA213.
LOT: 25KDB472
LOT: 26ADA161
LOT: 26ADB079
LOT: 26BDB740
LOT: 26DDA718
LOT: Lot Numbers: 26EDA285
LOT: UDI/DI 10198459266621 (each) 40198459266622 (case)
RECALL-NUMBER: Z-2764-2026

2. Is my exact product affected?

Compare every printed identifier. A matching value can indicate that your product is included.

3. What is the hazard?

4. What should I do now?

Follow the FDA recall notice and contact the recalling company for current instructions.

5. Where was it sold or distributed?

Colorado, Illinois

View source evidence for state distribution

Colorado: US: Mo, CO, IL
Illinois: US: Mo, CO, IL

6. Were injuries or illnesses reported?

No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.

7. What remedy is available?

Follow the FDA recall notice and contact the recalling company for current instructions.

8. Is the recall active or closed?

The source status is Ongoing. The Recall Guy's urgency label is urgent, which is a separate deterministic site label.

9. When was the information checked?

Last checked 10/1/2026, 7:00:04 PM UTC.

2026-10-01T19:00:04.000Zupdated
2026-10-01T19:00:04.000Zupdated
2026-10-01T15:00:04.000Zupdated
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2026-09-30T23:00:04.000Zupdated
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2026-09-30T10:00:21.000Zupdated
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2026-09-29T23:00:54.000Zupdated
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2026-09-29T19:00:54.000Zupdated
2026-09-29T19:00:54.000Zupdated
2026-09-29T15:00:54.000Zupdated
2026-09-29T15:00:54.000Zupdated

10. Where is the official source?

Open the official FDA Device source

The Recall Guy normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.