Medline Industries, Inc. DYNJ66447Recalls & reported problems
Medline Industries, Inc. · ENT ENDO SINUS WILMINGTON PACK · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name 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
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Mar 19, 2026Class IIOpen, Classified
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
Z-2023-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Nov 21, 2024Class IIOpen, Classified
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Z-0784-2025 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other Endoscope introducer kit devices
- Medline Industries, Inc. DYNJ44673GMedline Industries, Inc. · Endoscope introducer kit2 recalls0 reports
- Medline Industries, Inc. DYNJ58648JMedline Industries, Inc. · Endoscope introducer kit2 recalls0 reports
- ACS BUCY78EAmerican Contract Systems, Inc. · Endoscope introducer kit2 recalls0 reports
- ACS LVCY20AAmerican Contract Systems, Inc. · Endoscope introducer kit1 recall0 reports
- CARDINAL HEALTH PGVMDVB26Cardinal Health 200, LLC · Endoscope introducer kit1 recall0 reports
- CARDINAL HEALTH SOT51CPKOACardinal Health 200, LLC · Endoscope introducer kit1 recall0 reports
- CARDINAL HEALTH PGOCRDNHDCardinal Health 200, LLC · Endoscope introducer kit1 recall0 reports
- ACS HKCY31AAmerican Contract Systems, Inc. · Endoscope introducer kit1 recall0 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 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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