BBL™ CultureSwab™ EZ 220144Recalls & reported problems
Copan Italia SPA · BBL™ CultureSwab™ EZ CultureSwab EZ Swab Single · Class 1
Data updated Oct 16, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- May 2, 2025Open, Classified
Swabs for specimen collection may be prone to breakage during product usage.
Z-1937-2025 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other System, Transport, Aerobic devices
- BD Vacutainer® Urine Complete Cup Kit 364957Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC1 recall5 reports
- BD Vacutainer® Urine Transfer Straw 364966Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC22 reports
- BD Vacutainer® Urinalysis Cup Kit 364946Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC11 reports
- BD Vacutainer® Urinalysis Transfer Straw Kit 364990Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC11 reports
- BD Vacutainer® Urine Collection Cups 364975Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC10 reports
- BD Vacutainer® Urinalysis Transfer Straw Kit 364943Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC9 reports
- BD Vacutainer® Urinalysis Cup Kit 364981Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC5 reports
- BD Vacutainer® Urinalysis Cup Kit 364989Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC3 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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