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U.S. Department of Health and Human Services

Class 2 Device Recall BAIR PAWS TEMPERATURE MANAGEMENT SYSTEM MODEL 850

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 Class 2 Device Recall BAIR PAWS TEMPERATURE MANAGEMENT SYSTEM MODEL 850see related information
Date Initiated by FirmDecember 17, 2009
Date PostedMarch 01, 2010
Recall Status1 Terminated 3 on April 19, 2012
Recall NumberZ-0898-2010
Recall Event ID 54487
510(K)NumberK053645 K060865 
Product Classification system, thermal regulating - Product Code DWJ
ProductElectri-Cord Manufacturing Corporation(312 E. Main St., Westfield, PA 16950) AC power cords used with Ranger Pressure Infusion Power Pack; Model 90033. To provide power to pressure infusers.
Code Information Part number 502221 Model 90024
Recalling Firm/
Manufacturer
Arizant Inc
10393 W 70th St
Eden Prairie MN 55344
For Additional Information Contact
952-941-8866
Manufacturer Reason
for Recall
Arizant Healthcare Inc. is initiating a nationwide voluntary recall of 100/110-volt power cords (Arizant part number 502221 Model 90024) attached to its temperature management units and pressure infusion power pack (Bair Paws Temperature Management Units: Models 850 and 875 Bair Hugger Temperature Management Units: Models 500/OR, 505 (Human & Vet.), 750 (Human & Vet) and 775 Ranger Blood/Flui
FDA Determined
Cause 2
Nonconforming Material/Component
ActionAn "Urgent Medical Device Power Cord Recall" letter dated December 17, 2009 was sent to customers. The letter was addressed to Recall Coordinator/Biomed Dept. The letter described the affected product, problem, hazard involved, and action to be taken by customer. The customers are being ask to inspect their temperature management units (as described in FDA's recommendation dated October 19, 2009) and contact the firm with the results of their inspection and provide a contact name via website www.arizant.com/powercords or phone (877) 947-1487. Replacement cords and instructions will be provided to customers based on priority listed in the letter and availability of replacement cords. If the customer does not have the means to make the changes, alternate means will be taken (i.e., an Arizant employee or outside service organizations may be brought in to do the replacements). If you have any questions, please contact the Aziant at (877) 47-1487.
Quantity in CommerceTotal distributed for all devices: 84,537 US, 7,380 OUS.
DistributionWorldwide Distribution: USA and ARGENTINA, THE BAHAMAS, CANADA, COLOMBIA, COSTA RICA, CUBA, DOMINICAN REPUBLIC, ECUADOR, GERMANY, GUAM, JAPAN, LEBANON, MEXICO, NICARAGUA, PANAMA, PUERTO RICO, QATAR, SAUDI ARABIA, SOUTH KOREA, SURINAME , TAIWAN, TRINIDAD AND TOBAGO, QATAR.
Total Product Life CycleTPLC 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) Database510(K)s with Product Code = DWJ
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