Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; D...
FDA Recall #Z-1048-2024 — Class I — December 4, 2023
Product Description
Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 18 FR (6.0 MM), 5 CC, 2000 ML DRAIN BAG; Dover" HYDROGEL COATED LATEX FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML BAG, DRAIN SPOUT; Dover" URINE DRAINAGE ADD-A-FOLEY TRAY, LUER LOCK SAMPLING PORT, A/R DEVICE, DRAIN SPOUT, PREP TRAY; Dover" HYDROGEL COATED LATEX 400 ML U/M FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML BAG; Dover" UNIVERSAL TRAY, 1000 ML BASIN, BZK SWAB STICKS, PREPPING COMPONENTS, 10 ML PRE-FILLED SYRINGE; Dover" 100% SILICONE SILVER-HYDROGEL COATED 400ML U/M FOLEY TRAY, COUD¿ TIP, 16FR (5.3 MM), 5CC; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 18 FR (6.0 MM), 5 CC, 2000 ML DRAIN BAG (2-person); Dover" 100% SILICONE SILVER-HYDROGEL COATED 400ML U/M FOLEY TRAY, COUD¿ TIP, 18FR (6.0 MM), 5CC; Dover" PREMIUM URINE DRAINAGE ADD-A-FOLEY TRAY, LUER-LOCK, DRAIN SPOUT, CATHETER SECUREMENT DEVICE
Reason for Recall
Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
Recalling Firm
Cardinal Health 200, LLC — Waukegan, IL
Classification
Class I — Reasonable probability of serious adverse health consequences or death.
Product Type
Devices
Product Quantity
195600 units
Distribution
US and EMEA, Japan, Latin America
Code Information
a) P4P16CSDK, UDI/DI 20884521174068 (cs), 10884521174061 (ea), Lot Numbers: 2134218264, 2231213064, 2231213164, 2231901164, 2231901264, 2303822464, 2303007064, 2307110664, 2310808164, 2315609464, 2319100364, 2319213064, 2203300964, 2210218464, 2211031564, 2213045564, 2214449364, 2215824164, 2216500464, 2217920064, 2219400664, 2300202064, 2304400364, 2304400464, 2301703364, 2303006964, 2308700564, 2309041264, 2312206464, 2321324164, 2322006864, 2211626864, 2305206264, 2322102764, 2206726164, 2216805064, 2313615064, 2313614964, 2312908364, 2309041264, 2201151164, 2201201664, 2202401464, 2200603564, 2205315264, 2209524264, 2213738964, 2215117864; b) P4P18CSDK, UDI/DI 20884521174075 (cs), 10884521174078(ea), Lot Numbers: 2231213564, 2308004464, 2319100564, 2215824364, 2232517864, 2312206964, 2134218564, 2203931664
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated
What Should You Do?
Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.