BD Calibrated Disposable Inoculating Loops, Blue 220217Recalls & reported problems
Becton, Dickinson And Company · Loops Inoculating 50/Tube 10 Microliter · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00382902202172), received between Aug 7, 2023 and Nov 18, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (4 reports).
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.
Reports received per month
Most reported problems
Device problems
- Device Markings/Labelling Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 18, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED PRIOR TO USING BD CALIBRATED DISPOSABLE INOCULATING LOOPS THAT THE CASE WAS LABELED WITH THE 10UL PRODUCT INFORMATION BUT PACKED WITH THE 1UL PRODUCT. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20715472 ↗MalfunctionMar 4, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED WHEN USING THE BD CALIBRATED DISPOSABLE INOCULATING LOOPS, BLUE 10L (20X50 LOOPS) THERE WERE 10 MISLABELED BOXES. THERE WAS NO REPORT OF IMPACT TO THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18830128 ↗MalfunctionAug 9, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT WHILE USING BD CALIBRATED DISPOSABLE INOCULATING LOOPS, BLUE 10L (20X50 LOOPS), THE COC SHOWS INCORRECT LABEL INFORMATION. NO PATIENT IMPACT REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CUSTOMER REPORTS THAT THE COC SHOWS THE PRODUCT AS 1 UL AS OPPOSED TO 10 UL."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17495625 ↗MalfunctionAug 7, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT WHILE USING BD CALIBRATED DISPOSABLE INOCULATING LOOPS, BLUE 10L (20X50 LOOPS), THE COC LISTS INCORRECT LABEL INFORMATION. NO PATIENT IMPACT REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CUSTOMER REPORTS THAT COC LISTS 1 MICROLITER LOOPS INSTEAD OF 10."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17476494 ↗
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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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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