Medline Industries LP Recalls Convenience Kits
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Medline Industries, LP is recalling 2,301 convenience kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP due to quality issues from the manufacturer.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 12, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their supplier, Spectra Medical Devices, LLC of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues. The recall is classified as Class I and is ongoing.
Which Products Are Affected
The recall affects 2,301 kits distributed in OH, CA, IL, IN, FL, SC, AZ, and NJ. Affected products include 26 Medline Kit SKUs: DYKS1574A, DYNJ902378J, DYNJ903492K, DYNJ903493I, DYNJ903493J, DYNJ903493K, DYNJ906665G, DYNJ906666J, DYNJ909000A, DYNJ909002A, DYNJ909068B, DYNJ909069B, DYNJ909070C, DYNJ909071B, DYNJ909071C, DYNJ909534, DYNJ909534A, DYNJ909534B, DYNJ909640F, DYNJ909642D, DYNJ909643D, DYNJ909643F, DYNJ910002A, DYNJ910354A, DYNJ910813, and DYNJ911083. Specific lot numbers and UDI/DI codes are listed in the recall notice. Recall number Z-2749-2026.
What You Should Do
Consumers should follow instructions provided in notifications from Medline Industries, LP regarding the recalled kits.
Why This Matters
This Class I recall involves medical device kits used in surgical procedures and affects over 2,300 units across multiple states.
Source
FDA recall Z-2749-2026, report date 20260729.
Original source: FDA Official Notice ↗
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