Recall of LSL Healthcare Foley Urine Collection 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 100 units of their Foley Urine Collection Kit due to included alcohol prep pads that were recalled for non-sterility.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 7, 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, cpsc, Devices.
What Happened
LSL Healthcare Inc. is recalling their Foley Urine Collection Kit because the kits contain Webcol Large Alcohol Prep Pads that were previously recalled for not being sterile.
Which Products Are Affected
The affected product is the LSL Healthcare Foley Urine Collection Kit, Model/Catalog Number: 1555. Approximately 100 units are involved, with distribution in the states of MD, IL, and MN across the US. The lot code is 260221, expiration date is February 28, 2027, UDI-DI: 00661392002326, and GTIN: (01)00661392002326(10)260221(17)270228.
What You Should Do
The recall was initiated via E-Mail by the firm. Consumers with the affected kits should contact LSL Healthcare Inc. for further instructions on returns or refunds.
Why This Matters
This recall affects medical devices that may not be sterile, potentially posing health risks, though the FDA classifies it as Class II, indicating a remote probability of serious adverse health consequences.
Source
This information is from the FDA recall notice, recall number Z-1930-2026. For more details, visit the FDA website.
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 (1,105 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 7, 2026.
Frequently Asked Questions
Common questions about this FDA recall.