FDA recall record

Teleflex Medical Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only recall — FDA Z-2251-2017

Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.

Class IIclassification
Z-2251-2017official record ID
Jun 14, 2017report date

Recall record at a glance

Official recordZ-2251-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTeleflex Medical
Report dateJun 14, 2017
Recall initiation dateMay 9, 2017
Quantity1150 units
LocationResearch Triangle Park, NC, United States

Official product description

Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,

Why the product was recalled

Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.

Distribution information

CA, CT, FL, IL, IN, MD, MI, MN, MO, MS, NC, NJ, NY, NV, OH, PA, TX, VA, WI and WV.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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