Recall of Philips S5-2 Ultrasound Transducer Issued
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Philips Ultrasound, Inc. is recalling one unit of the Philips S5-2 Ultrasound Transducer to provide clarification on its useful life, as announced by the FDA.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 8, 2026 and geographically references United States. Its severity classification of "low" 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.
What Happened
The recall was initiated to provide clarification and labeling to define the useful life of the ultrasound transducers in the field.
Which Products Are Affected
The affected product is the Philips S5-2 Ultrasound Transducer. It includes Model No. 989605368393 and Serial No. B0C824. The quantity involved is 1 unit, with distribution occurring nationwide in the United States.
What You Should Do
Consumers who have the affected product should contact Philips Ultrasound, Inc. for further instructions, as the recall was initiated via letter.
Why This Matters
This recall ensures that users have accurate information on the useful life of medical devices, helping to maintain safety and proper functionality in healthcare settings.
Source
FDA recall notice Z-1626-2026. For more information, visit the FDA website at https://www.fda.gov.
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 (869 characters here).
Similar severity timing
Same severity (low) notices issued closest in time to April 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.