Cardinal Health 200 recalls
27 recent recalls on record for Cardinal Health 200 in connected official government data as of October 22, 2026 at 12:00 PM UTC.
Models with recalls
All Cardinal Health 200 recalls
FDA Class II · Medical device · October 14, 2026
Kits contain Microstream components. Medtronic issued an update to the Instructions for Use of these components due reports of difficulty in disconnecting the adapter from the pati…
Official ID Z-0079-2027 ·
Official record ↗
FDA Class II · Medical device · October 7, 2026
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Official ID Z-3298-2026 ·
Official record ↗
FDA Class II · Medical device · October 7, 2026
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Official ID Z-3297-2026 ·
Official record ↗
FDA Class II · Medical device · October 7, 2026
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Official ID Z-3296-2026 ·
Official record ↗
FDA Class II · Medical device · October 7, 2026
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the fl…
Official ID Z-3295-2026 ·
Official record ↗
FDA Class II · Medical device · September 30, 2026
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient…
Official ID Z-3255-2026 ·
Official record ↗
FDA Class II · Medical device · September 30, 2026
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient…
Official ID Z-3254-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3105-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3104-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3103-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3102-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3101-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3100-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3099-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3098-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3097-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3096-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3095-2026 ·
Official record ↗
FDA Class II · Medical device · September 9, 2026
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is…
Official ID Z-3094-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2949-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2948-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2947-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2946-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2945-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2944-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2943-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Official ID Z-2942-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.