Recall of LSL Healthcare IV Start Kit
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
LSL Healthcare Inc. is recalling 2200 units of its IV Start Kit due to the inclusion of potentially non-sterile alcohol prep pads.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 8, 2026 and geographically references United States. Its severity classification of "medium" 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, Devices.
Recall of LSL Healthcare IV Start Kit
What Happened
LSL Healthcare Inc. is recalling medical procedure kits because they contain Webcol Large Alcohol Prep Pads that were previously recalled for non-sterility.
Which Products Are Affected
The affected product is the LSL Healthcare IV Start Kit, Model/Catalog Number: 3131. A total of 2200 units are involved, with Lot Code: 6A3139 and Expiration Date: 01/21/2028. The product has UDI-DI: 00661392054271 and GTIN: (01)00661392054271(10)6A3139(17)280121. Distribution occurred nationwide in the United States, specifically in the states of MD, IL, and MN. The recall number is Z-1932-2026.
What You Should Do
Consumers should contact LSL Healthcare Inc. for instructions, as the recall was initiated via e-mail notification.
Why This Matters
This recall addresses potential risks associated with non-sterile medical devices, which could affect patient safety in healthcare settings.
Source
FDA recall notice Z-1932-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (989 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.