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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73696

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 30, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Amd-Ritmed, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

AMD-RITMED brand Conforming Stretch Gauze Bandages, Sterile, 6 in x 4/1 yds./15 cm x 3.7 cm, Reorder Number/Code D606, Bar code 6 86864 04230 3, Made in China -- Manufactured for & distributed by: AMD-RITMED INC. Montreal Quebec H8T 3J8 -- US Distribution: AMD-RITMED INC. Tonawanda, NY 14150 -- Type of packaging: 1 roll/pouch, 12 pouches/inner box, 4 inner box/case, 48 rolls per case. Conforming bandages used to cover and protect wounds from further injuries and contamination. This type of product fits all parts of the body without restrictive movement. To be used in health care facilities.

Z-2213-2016
Recall number
Z-2213-2016
Initiated
March 30, 2016
Classification
Class II
Status
Terminated
Recalling firm
Amd-Ritmed, Inc.
Quantity
US: 107 cases (48 rolls per case)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The product lot did not meet sterility requirements based on FDA sampling and analysis.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Material/Component Contamination

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The product lot did not meet sterility requirements based on FDA sampling and analysis.

Code information

Lot 64155, Expiration Date 2017-06

Distribution pattern

US Distribution in states of: NY, CA, and TN.

Field note

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