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A woman who developed a rare type of cancer linked to her implants has warned that others with similar implants could be walking around like timebombs. Susan Axelby, 68, was recently paid 57,000 by Allergan Limited after she fell ill with -implant associated anaplastic large-cell lymphoma (BIA-ALCL).
NBIR is the only clinical data registry named by the FDA in all implant device labeling and safety communications. NBIR supports validated device tracking with built-in Global Unique Device Identification Database (GUDID) technology.
Due to the low risk of developing BIA-ALCL, the FDA does NOT recommend having your implants removed unless you are experiencing symptoms, which include pain, lumps, swelling, fluid collections or unexpected changes in shape, including asymmetry. If this is the case, contact a board-certified plastic surgeon.
🚨 Airport Security Scanners implants may be detected in body scanners but will not trigger alarms. Security staff are trained in handling medical implants professionally. 📝 Carry a Medical Note (Optional) If concerned, ask your surgeon for a letter confirming you have implants.
Qid technology, or Q Inside Safety technology, is used in Motiva Implants to provide an extra layer of safety for patients. Qid is a microtransponder or microchip, embedded within Motiva implants. This technology holds comprehensive details about the Implant, including: Implant Brand.
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