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U.S. Department of Health and Human Services

Class 2 Device Recall

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  Class 2 Device Recall see related information
Date Initiated by Firm December 30, 2003
Date Posted January 16, 2004
Recall Status1 Terminated 3 on July 21, 2004
Recall Number Z-0354-04
Recall Event ID 28030
Product Classification Thermometer, Electronic, Clinical - Product Code FLL
Product Sure Temp Plus Model 690/692 Oral Temperature Probes
Code Information Welch Allyn¿ Part #s: 0690-XXX Serial Numbers/Lot Numbers 02692-000 Oral Probe 4 ft. 412003-442003, 472003, 522003-582003. 02692-100 Oral Probe 9 ft. 412003-442003, 472003, 522003-582003 02893-000 Oral Probe Well Kit 4 ft. 412003-442003, 472003, 522003-582003 02893-100 Oral Probe Well Kit 9 ft. 412003-442003, 472003, 522003-582003    Probes are contained in Welch Allyn¿ Thermometer Boxes with Part #s: 0690-XXX Serial Numbers/Lot Numbers 01690-000 03397655 - 03505486 01690-200 03397655 - 03505486 E-01690-200 03397655 - 03505486 01690-300 03397655 - 03505486 01690-400 03397655 - 03505486 01690-410 03397655 - 03505486 01690-500 03397655 - 03505486 E-01692-200 03397655 - 03505486 01692-200 03397655 - 03505486 01692-300 03397655 - 03505486 01692-400 03397655 - 03505486 01692-500 03397655 - 03505486 01692-700 03397655 - 03505486    Probes are contained in Welch Allyn¿ Vital Signs Monitor III boxes with Part#s: Serial Numbers/Lot Numbers 53NTO-E1 JA000244, JA000282, JA000283, JA000284,  JA000285, JA000286, JA000287, JA000288, JA000289, JA000290, JA000291, JA000292, JA000293, JA000294, JA000295, JA000296, JA000297, JA000298, JA000299, JA000300, JA000301, JA000302, JA000303, JA000304, JA000305, JA000306, JA000307, JA000308, JA000309, JA000310, JA000311, JA000312, JA000313, JA000314, JA000315, JA000316, JA000317, JA000318, JA000319, JA000320, JA000331, JA000332, JA000333, JA000334, JA000335, JA000336, JA000337, JA000340, JA000341, JA000342, JA000343, JA000344, JA000345, JA000347, JA000348, JA000349, JA000352, JA000353, JA000354 53NTP-E1 JA000232, JA000243, JA000246, JA000255, JA000258, JA000259, JA000271, JA000278, JA000281, JA000326, JA000327, JA000328, JA000357 
Recalling Firm/
Manufacturer		 Welch Allyn Inc
7420 Carroll Rd
San Diego CA 92121-2334
For Additional Information Contact Debra Jackson
858-621-6600
Manufacturer Reason
for Recall		 Mechanical setting errors that result in calibration errors.
FDA Determined
Cause 2		 Other
Action Recall letters dated 12/29/2003 were sent to all customers requesting quarantine and subrecall if needed. Consignees are to request return authorization for replacement.
Quantity in Commerce 4453
Distribution Nationwide
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.
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