Medline Industries, LP recalled 596 Medline kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light may fail to illuminate as designed. Healthcare providers should stop using the devices immediately and follow recall instructions.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Medline kits are used in medical settings to aid airway management. They include Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. These kits support clinicians during intubation.
If the light in the laryngoscope handle does not illuminate, clinicians may have difficulty visualizing the airway. This could delay or complicate airway management.
This recall is not part of a broader industry pattern.
Healthcare facilities may need to substitute devices or delay procedures. The risk is situational and depends on the urgency of airway management.
Model numbers are printed on kit labeling and packaging.
4-6 weeks for refunds or replacements typical in recalls.
Keep copies of recall notices, model numbers, lot numbers, and all correspondence with Medline
Quick-reference: - ACC010381C NEWBORN RESUSCITATION KIT - ACC010532 DRAWER 5 - POSITION 3 - ACC010671 DRAWER #4C ADULT - ACC010728 DRAWER #2 Distribution: US distribution to AL, CA, DE, OR, TN, TX When sold: Unknown Price: Unknown
No injuries or incidents have been reported.
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