Z-1422-04

Allegiance Laminated Crutch Accessories, item 74152-010, Allegiance Crutch Underarm Pad; 2 pads per package...

Name: Z-1422-04 Allegiance Laminated Crutch Accessories, item 74152-010, Allegiance Crutch Underarm Pad; 2 pads per package...
Creator: Duro-Med Industries, Inc.
Published: 2004-08-04
License: https://open.fda.gov/license/

Duro-Med Industries, Inc. / initiated 2004-08-04 / Terminated / root cause: labeling and UDI

FDA source

Duro-Med Industries, Inc. began a recall of Allegiance Laminated Crutch Accessories, item 74152-010, Allegiance Crutch Underarm Pad; 2 pads per package, 12 packages per case; Distributed by Cardinal... on 2004-08-04. The reason FDA records is "The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-1422-04
Status: Terminated
Initiated: 2004-08-04
Posted: 2004-09-01
Terminated: 2006-03-24
Recalling firm: Duro-Med Industries, Inc.
Product: Allegiance Laminated Crutch Accessories, item 74152-010, Allegiance Crutch Underarm Pad; 2 pads per package, 12 packages per case; Distributed by Cardinal Health, McGaw Park, IL 60085-6787 USA, Made in China
Product code: INP Tips And Pads, Cane, Crutch And Walker
Reason for recall: The crutches were labeled as latex free, but contain rubber in the hand grips, tips and underarm padding of the crutches.
Root cause tag: labeling and UDI
FDA root cause: Other
Action: Duro-Med notified Cardinal Health of the recall by letter dated 8/4/04. Cardinal Health initiated a sub-recall of the products by letter dated 8/18/04. The accounts were informed that the products made in China contain latex, and were requested to check their inventories for the affected products and return those products found to be labeled as 'Made in China' for credit. Questions were directed to Cardinal Quality Systems at 1-800-292-9332.
Quantity in commerce: 6 cases
Distribution: Nationwide distribution through Cardinal Health.
Product codes and lots: catalog #74152-010, all product labeled ''Made in China''

Product code INP

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)