Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1783-2020Class II

Temperature Sensing 100% Silicone Foley Catheter, Part Number 102201101663MD -

Degania Medical Devices Pvt. Ltd. / initiated 2020-03-17 / Terminated / root cause: manufacturing process

Degania Medical Devices Pvt. Ltd. began a recall of Temperature Sensing 100% Silicone Foley Catheter, Part Number 102201101663MD - Product Usage: is a 3 lumen silicone catheter with a sensor to measure... on . FDA classified it as Class II and gives the reason as "Inadequate incoming inspection practices were utilized on thermistor sensors used in the production of the specified lots of temperature sensing catheters". As of , the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-1783-2020
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Degania Medical Devices Pvt. Ltd.
Product
Temperature Sensing 100% Silicone Foley Catheter, Part Number 102201101663MD - Product Usage: is a 3 lumen silicone catheter with a sensor to measure temperature while draining the urinary bladder.
Product code
EZL Catheter, Retention Type, Balloon
Reason for recall
Inadequate incoming inspection practices were utilized on thermistor sensors used in the production of the specified lots of temperature sensing catheters.
Root cause tag
manufacturing process
FDA root cause
Nonconforming Material/Component
Action
An Urgent Field Safety Notice dated 3/17/20 was sent to customers. Please immediately follow the Required Customer Actions set fo rth below. 1. Please forward this information to the immediate attention of the persons responsible for usage of the affected parts. Sub-recall must be initiated by your company to collect any distributed product from the suspected list. 2. Please fill in the attached Recall Response form and indicate the quantity of the affected product in your possession. 3. Please promptly return the completed Recall Response fo rm to Degania Silicone by e-mail: [email protected]. 4. The disposition of the recalled goods should be scrap. We would ask you to destruct the goods at your facil ity and send us the Scrap confirmation letter. Should you have any questions about this subject, please contact Degania Silicone: Degonia Silicone Ltd. Degania Bet, 1513000, ISRAEL Katia Kayam, Cust omer compla ints Officer Tel: +972-529532059 E-mail: [email protected]
Quantity in commerce
52566
Distribution
Worldwide distribution - US Nationwide distribution including state of IL and the country of Mexico.
Product codes and lots
Lot Numbers: V18007422 V18010291 V18023106 V18023107 V18023108 V18023109 V18025115 V18025117 V18025118 V18025119 V18026073 V18037032 V18026072 V18035228 V18035229 V18036131 V18037031 V18037033 V18037938 V19001678 V19001679 V19002478 V19002479 V19002480 V19013333 V19025876 V19026564 V19027234 V19027235 V19016726

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1783-2020
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1779-2020Class IITerminatedVoluntary: Firm initiated
Z-1780-2020Class IITerminatedVoluntary: Firm initiated
Z-1781-2020Class IITerminatedVoluntary: Firm initiated
Z-1782-2020Class IITerminatedVoluntary: Firm initiated
Z-1783-2020Class IITerminatedVoluntary: Firm initiated
Z-1784-2020Class IITerminatedVoluntary: Firm initiated
Z-1785-2020Class IITerminatedVoluntary: Firm initiated
Z-1786-2020Class IITerminatedVoluntary: Firm initiated
Z-1787-2020Class IITerminatedVoluntary: Firm initiated
Z-1788-2020Class IITerminatedVoluntary: Firm initiated
Z-1789-2020Class IITerminatedVoluntary: Firm initiated