Halyard Pain Pack Recall Issued by AVID Medical
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
AVID Medical, Inc. is recalling 120 Halyard Pain Pack kits distributed nationwide due to unsterilized pouches.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 28, 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.
What Happened
AVID Medical, Inc. initiated a voluntary recall of Halyard Pain Pack kits after discovering that sealed pouches had not undergone validated sterilization.
Which Products Are Affected
The recall involves Halyard, Pain Pack, Kit Code: AMPK48-01. Affected units include Lot Number: 334669 with UDI-DI: 10809160472798 and Expiration Date: 8/27/2028. A total of 120 kits were distributed. Distribution was to US Nationwide in the state of Iowa. The recall number is Z-2407-2026. The recall is classified as Class II and remains ongoing.
What You Should Do
Consumers and healthcare providers should check inventory for the affected lot and follow instructions provided by the recalling firm.
Why This Matters
The distribution of unsterilized medical kits poses a potential risk of infection to patients.
Source
FDA recall Z-2407-2026 (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 (882 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 28, 2026.
Frequently Asked Questions
Common questions about this FDA recall.