CARDINAL HEALTH SMAHBCSECBRecalls & reported problems
Cardinal Health 200, LLC · C SECTION PACK · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jul 29, 2026Open, Classified
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 used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.
Z-3102-2026 · Root cause: Process change control · FDA record ↗
Other Cesarean section tray devices
- Medline Industries, Inc. DYNJ32632FMedline Industries, Inc. · Cesarean section tray4 recalls0 reports
- Medline Industries, Inc. DYNJ904697FMedline Industries, Inc. · Cesarean section tray4 recalls0 reports
- Medline Industries, Inc. DYNJ33059BMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ9932207RMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. CDS820075WMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ15494GMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ83507Medline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ47808FMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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