Atlas FDA

Infant reusable blood pressure cuffs, one tube, male slip luer connector, P/N 2930 , manufactured for Welch Allyn Protoc

FDA device recall Z-1237-03 · posted 2003-10-15 · Terminated

Recall details

Recalling firm
GE Medical Systems Information Technologies
Reason for recall
Wrong connector attached to blood pressure cuff.
Action taken
The recalling firm telephoned the one account involved on 3/7/2001 and also mailed a Recall Notification letter to the firm on 3/7/2001 requesting return of the product.
Root cause
Other
Status
Terminated
Quantity affected
100 cuffs
Distribution
Product was distributed to one distributor in Oregon.
Date initiated
2001-03-07
Date posted
2003-10-15
Date terminated
2008-04-15
Location
Tampa, FL

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