Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A
Reported: February 26, 2025 Initiated: January 9, 2025 #Z-1182-2025
Product Description
Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A
Reason for Recall
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
Details
- Recalling Firm
- MEDLINE INDUSTRIES, LP - Northfield
- Units Affected
- 70 kits
- Distribution
- US States: CA, NY
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 70 kits.
Why was this product recalled? ▼
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 26, 2025. Severity: Moderate. Recall number: Z-1182-2025.
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