Z-0004-2013Class II

Male, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in...

Name: Z-0004-2013 Male, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in...
Creator: Cure Medical LLC
Published: 2012-09-19
License: https://open.fda.gov/license/

Cure Medical, LLC / initiated 2012-09-19 / Terminated / root cause: labeling and UDI

FDA source

Cure Medical LLC began a recall of Male, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in intermediate boxes containing 30 individual, sterile... on 2012-09-19. FDA classified it as Class II and gives the reason as "The firm initiated the product recall because labeling on some of the intermediate boxes of catheters identify the contents to be M16C, a coud-tip catheters while the actual contents are M16Fr male, 16Fr, straight-tip...". 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-0004-2013
Classification: Class II
Status: Terminated
Initiated: 2012-09-19
Posted: 2012-10-02
Terminated: 2013-02-07
Recalling firm: Cure Medical, LLC
Product: Male, 16Fr, Straight-tip Intermittent Urinary Catheters M16. The product is distributed individually or in intermediate boxes containing 30 individual, sterile packaged catheters (PA/PE film and dialyzing paper pouches). There are 30 catheters packaged in sterile pouches that are placed into an intermediate box, 10 of these intermediate boxes packaged into one case. K072539 The Cure Catheter" device, M16, is an intermittent urinary catheter intended to be used by males for the purpose of bladder drainage. It is manufactured with conventional medical grade, latex-free, biocompatible materials. The straight-tip has been designed to eliminate trauma to the urethra and is provided in 16Fr size in an easy-to-open, sterile, single-use package. The coud-tip catheter, M16C, is designed with a curved tip that makes it easier to pass through the curvature of the prostatic urethra in men. It is also used to pass through urethral strictures. This product is prescribed for people who have difficulty or are unable to pass a straight catheter through their urethra and into their bladder.
Product code: EZD Catheter, Straight
Reason for recall: The firm initiated the product recall because labeling on some of the intermediate boxes of catheters identify the contents to be M16C, a coud-tip catheters while the actual contents are M16Fr male, 16Fr, straight-tip catheters with the pouch and the case box labeled as M16Fr male, 16Fr, straight-tip catheters.
Root cause tag: labeling and UDI
FDA root cause: Labeling mix-ups
Action: Cure Medical LLC sent an Urgent Medical Device Correction and Removal Notification letter dated September 19, 2012, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. The letter instructed the customers to: a) Check their shelves for M16C with lot number 120425 and quarantine all affected product. b) Verify the contents (pouch label) are M16C and correspond with the intermediate box label. c) If all match, have the dealer sign and return a supplied verification record. d) If any mismatch is found, contact Cure Medical for assignment of a return goods authorization. e) Cure Medical will replace any incorrect product along with processing costs for this situation to the dealer. If affected product was further distributed customers were asked to identify those customers who received them and notify them of the problem. For questions customers were instructed to call 1-800-570-1778.
Quantity in commerce: 420cases (= 4,200 boxes)
Distribution: Nationwide Distribution
Product codes and lots: Total affected product: M16, Lot 120425: 420 cases = 4,200 boxes = 126,000 each. 2017.03 is shown on the product labeling as the expiry date for the product, 4 years and 11 months from the date of packaging. The product, M16, is identified with the following UPC Codes for the individual pouches, intermediate boxes and case labels: ¿ Pouch Label UPC (M16) = *+M405M16 ¿ Box Label UPC (M16) = *+M405M163I* " Case Label UPC (M16) = *+M405M165K* Explanation of Lot Number: The lot number represents a planned packaging date of a set of work orders for various products, in the format YYMMDD at the contract manufacturers facility. At the order planning stage, the packaging date is estimated (based on production cycle time and pre-printed box delivery) and assigned to each work order The lot number represents a planned packaging date of a set of work orders for various products, in the format YYMMDD at the contract manufacturers facility. At the order planning stage, the packaging date is estimated (based on production cycle time and pre-printed box delivery) and assigned to each work order scheduled for packaging on this estimated date. Therefore, one lot number may be assigned to multiple catalog numbers. The lot number 120425 was assigned to both M16 and M16C products by the scheduling department Actual packaging of the M16 occurred from 23 May 2012 through 25 May 2012. Actual packaging of the M16C occurred from 19 May through 21 May 2012.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0004-2013
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0004-2013	Class II	Terminated	Voluntary: Firm initiated	2012-10-10	2012-10-02

Product code EZD

K072539Class IICure CatheterCure Medical, LLC / cleared 2007-09-13

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)