3M™ Attest™ 1243BRecalls & reported problems
3m Company · 3M™ Attest™ Steam Chemical Integrator, 1243B, Type 5, 3/4 in x 2 in (1.9cm x 5.1 cm), 100/BAG, 10 BAG/CS, 1000/CS · Class 2
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
- Apr 6, 2023Open, Classified
3M Attest Steam Chemical Integrators with dates of manufacture between November 6, 2022 and January 17, 2023 have an increased potential to leak ink during a sterilization cycle.
Z-1610-2023 · Root cause: Process control · FDA record ↗
Other Indicator, physical/chemical sterilization process devices
- Integron® IT26-CTerragene S.A. · Indicator, Physical/Chemical Sterilization Process1 recall5 reports
- BENCO 5726-583Benco Dental Supply CO. · Indicator, Physical/Chemical Sterilization Process1 recall0 reports
- 3M™ Attest™ 1243A3m Company · Indicator, physical/chemical sterilization process1 recall0 reports
- DH Nyclave Indicator Labels 116312Young Dental Manufacturing I, LLC · Indicator, Physical/Chemical Sterilization Process1 recall0 reports
- Comply™ 12483m Company · Indicator, physical/chemical sterilization process1 recall0 reports
- Comply™ 12483m Company · Indicator, physical/chemical sterilization process1 recall0 reports
- Integron® IT26-CTerragene S.A. · Indicator, Physical/Chemical Sterilization Process1 recall0 reports
- VERIFY SixCess LCC003Steris Corporation · Indicator, physical/chemical sterilization process1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.