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U.S. Department of Health and Human Services

Class 1 Device Recall WOLFPAK, Medpro, Vipat

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  Class 1 Device Recall WOLFPAK, Medpro, Vipat see related information
Date Initiated by Firm July 09, 2011
Date Posting Updated October 30, 2012
Recall Status1 Terminated 3 on September 22, 2014
Recall Number Z-0161-2013
Recall Event ID 60030
510(K)Number K081905  
Product Classification Pump, infusion, elastomeric - Product Code MEB
Product Medpro Elastomeric Infusion Pump.

AccuFlux, Model # CT-0020-100H.

Product Usage:
The devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications. It is the responsibility of the user to ensure that the medication is prepared and administered accordance with the drug manufacturers package insert. The devices deliver controlled amounts of medication directly to the intraoperative site for pain management and or antibiotic administration. The devices infuse the medication at an hourly flow rate. Medications are infused intraoperatively and postoperatively through intramuscular or subcutaneous routes. The devices are also intended for controlled delivery of local anesthetics in close proximity to nerves for post operative regional anesthesia and pain management. Routes of administration may be intraoperative or percutaneous. It is for continuous infusion of medications for general infusion use, including antibiotic delivery and chemotherapy.
Code Information AccuFlux, Lot#: 91209.
Recalling Firm/
First Medical Source LLC
28581 Springfield Dr
Laguna Beach CA 92677-1424
For Additional Information Contact
Manufacturer Reason
for Recall
Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being reclassified by the Agency as a Class I. The recall was initiated because First Medical Source has confirmed that these lots may have a higher flow rate than specified. The use of this product may lead to over-administration of drug solutions to the patients. The pr
FDA Determined
Cause 2
Nonconforming Material/Component
Action Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being reclassified by the Agency as a Class I. First Medical Source received an email from Medpro International with the following lnstruction to Customer - Informed customers to remove product from sales/discontinue use, cease distribution, remove the products from inventory and quarantine, inform their customers to retum the unused products to them, and destroy the product. Distributors' customer service will contact the customer to coordinate the return of the goods in question where required. First Medical Source emailed to their customer, Williams Medical Technologies, to informed them of the recall of the Medpro Elastomeric infusion pumps. Customer was instructed to inform them of the date and method of disposal of recalled products.
Quantity in Commerce 500 units
Distribution US Nationwide distribution in the state of IL
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = MEB and Original Applicant = Westmed, Inc.