medical MODERATE Updated 2017-06-14

Teleflex Medical recalls Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx o

See all recalls from Teleflex Medical →

Recalled Product

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

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

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

Issued by

FDA

Affected States: CA, CT, FL, IL, IN, MD, MI, MN, MO, MS, NC, NJ, NY, NV, OH, PA, TX, VA, WI, WV
Lot/Code Info: Product Code: 1101, Lot numbers: 74J1603122, 74K1601506, 74K1602306 and 74L16006.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Hudson RCI, Pediatric Nasal →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Baxter Healthcare Corporation recalls Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Cir

2026-07-08 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

Medline Industries, LP recalls Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY,

2026-07-08 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Medline Industries, LP recalls Medline Convenience Kits: 1) MULTIMED, 7FR, 20CM, 3L, CVC B

2026-07-08 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circ

2026-07-08 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.