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Terminated

Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209

FDA Recall Z-2365-2015 · Posted 2015-08-10

Recalling FirmCadence Inc.
Recall StatusTerminated
Product CodeGAA
Date Initiated2015-07-09
Date Terminated2016-07-29
Product Quantity1665 units

Reason for Recall

Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

Firm Action

Cadence issued the recall letter, specific to the customer dated 7/9/15 via registered mail on July 17, 2015. Accounts are requested to Recalled products must not be used. 2. Locate and quarantine all affected products. 3. Contact Cadence Science, Inc. using the Response Form provided. 4. If this information is received by a dealer, wholesaler, or distributor/reseller that distributed any of these products to other facilities, then notify their customers of this action so that those customers can locate and remove all affected products. Any questions contact: Phone: 401-942-1031

Root Cause

Device Design

Distribution Pattern

Nationwide Foreign Canada, Denmark. Italy

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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