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

FDA device recall Z-2365-2015 · posted 2015-08-10 · Terminated

Recall details

Recalling firm

Cadence Inc.

Reason for recall

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

Action taken

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

Status

Terminated

Product code

GAA

Quantity affected

1665 units

Distribution

Nationwide Foreign Canada, Denmark. Italy

Date initiated

2015-07-09

Date posted

2015-08-10

Date terminated

2016-07-29

Location

Cranston, RI