Atlas FDA

Battery-operated Cautery Low Temperature, fine/elongated Tip

FDA device recall Z-1238-04 · posted 2004-08-04 · Terminated

Recall details

Recalling firm
Aaron Medical Industries, Inc.
Reason for recall
The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.
Action taken
Each consignee will be notified by letter of the recall with instruction for the disposal of the product determined to be hazardous. Each letter will have a questionnaire attached with a 800 fax number for replying to the firm.
Root cause
Other
Status
Terminated
Product code
HQP
Quantity affected
16700
Distribution
Distributed to: 291 accounts in the USA, 8 in Canada, 18 in Europe, 1 in the Middle East, 1 in Asia, 4 in the Pacific Rim 1 in Africa and 5 US goverment/Military.
Date initiated
2004-06-29
Date posted
2004-08-04
Date terminated
2012-05-03
Location
St Petersburg, FL

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