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Limited official informationFDA Medical Device Enforcement ReportsRecall date: Jun 17, 2026

Halyard, Towel Six Pack. Kit Code: AMTS70-01.

Full official product description

Halyard, Towel Six Pack. Kit Code: AMTS70-01. | Halyard, Pain Pack. Kit Code: AMPK48-01. | Halyard, Drape Pack. Kit Code: LMDP36-01. | Halyard, Eye Bag Pack. Kit Code: UIEB48-01.

Verification delayed

The last verified facts remain visible. Last successful verification: Aug 1, 2026, 3:43 PM UTC. A temporary source failure does not mean the recall changed.

Official information is incomplete

Missing: action, consumer scope. The page is public for lookup but excluded from search indexing and advertising.

1Is my item affected?

Compare the complete identifiers. Name similarity alone is not a confirmed match.

Halyard, Towel Six Pack. Kit Code: AMTS70-01.; Halyard, Pain Pack. Kit Code: AMPK48-01.; plus 2 additional official variants listed below.

Identifiers to compare

  • UDI 10809160469972
  • UDI 10809160472798
  • UDI 10809160479148
  • UDI 10809160484098
  • Lot AMTS70-01.
  • Lot 334669.
  • Lot LMDP36-01.
  • Lot UIEB48-01.
  • Lot AMTS70-01
  • Lot 334669
  • Lot LMDP36-01
  • Lot UIEB48-01

4 official variants

Affected variants from the official event record
Product or modelCodes and lotsQuantityRecall number
Halyard, Towel Six Pack. Kit Code: AMTS70-01.Kit Code: AMTS70-01. UDI-DI: 10809160469972. Lot Number: AMTS70-01. Expiration Date: 9/2/2028.224 kitsZ-2408-2026
Halyard, Pain Pack. Kit Code: AMPK48-01.Kit Code: AMPK48-01. UDI-DI: 10809160472798. Lot Number: 334669. Expiration Date: 8/27/2028.120 kitsZ-2407-2026
Halyard, Drape Pack. Kit Code: LMDP36-01.Kit Code: LMDP36-01.UDI-DI: 10809160479148. Lot Number: LMDP36-01. Expiration Date: 9/10/202872 kitsZ-2409-2026
Halyard, Eye Bag Pack. Kit Code: UIEB48-01.Kit Code: UIEB48-01. UDI-DI: 10809160484098. Lot Number: UIEB48-01. Expiration Date: 8/7/2028.60 kitsZ-2410-2026

2What is the risk?

The agency's statement is shown without a site-authored severity score.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Agency classification: Class II

3What should I do?

Only instructions associated with this recall event qualify as an action.

Consumer action is not available in the associated official record. The site does not infer or generate a replacement.

Verify on the official source

The linked agency record controls if any information differs.

Official evidence

Official scope

Distribution reported by the agency

US Nationwide distribution in the state of Iowa.

Distribution is context, not a confirmed item match. Compare the model, lot, UPC, NDC, or serial number above.

Material change history

  • : affectedSummary changed in the official record.