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Last updated: 2021
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Please note: using the search filters may not provide accurate search results for records prior to November 2021. When searching for older records, please ensure that you use the include archived checkbox.
Displaying 1 - 15 of 486 items.
Internal testing determined that magnesium failed to meet the interference claim as per ifu for the lipemic serum interference. all lots of magnesium osr6189 are affected.
Recall start date: 2021-12-06…
RecallHealth product recall | 2021-12-31
The OER-elite is intended for use in cleaning and high-level disinfection of heat sensitive Olympus flexible endoscopes, their accessories, and endoscope reprocessor accessories. Olympus discovered the detergent and alcohol tank tubing…
RecallHealth product recall | 2021-12-31
When the specific circumstances described below occur, there is a possibility of displaying distorted images along with erroneous measurements. the distortion and measurement difference could affect decisions regarding patient care.…
RecallHealth product recall | 2021-12-31
System overestimates the circumference when the manual trace function is used. the trace circumference value is overestimated; however, the area value is accurate. the issue is present in Sequoia's VA20A/VA25 onward as the VA20A introduced a…
RecallHealth product recall | 2021-12-31
No stability data to support affected lots' shelf life.
Affected lots are labelled with the incorrect expiry date found on the container
RecallHealth product recall | 2021-12-30
Contamination with ethylene oxide
RecallHealth product recall | 2021-12-30
Affected lot is labelled with unauthorized claims and ingredients including cetylpyridinium chloride. The product lablel is missing risk statements, the NPN and is incorrectly labelled for use in children.
RecallHealth product recall | 2021-12-24
If prior to the IFR/FFR pullback on the intrasight system, FFR measurement(s) were performed within the same syncvision procedural session, the co-registered distal value will be different than the distal value displayed in the philips IFR/FFR system.…
RecallHealth product recall | 2021-12-23
This face mask was evaluated as "filtration efficiency has not been verified" and it should not be used as a respirator.
Recall start date: Dec 13, 2021
RecallHealth product recall | 2021-12-23
The subject product is being removed because Deputy (Ireland) has determined that select lots of global unite stems may have an undersized spigot bore diameter.
Recall start date: Dec 13, 2021
RecallHealth product recall | 2021-12-23
The affected lots could contain type DA-2I ethanol.
RecallHealth product recall | 2021-12-22
Medtronic has identified an anomaly with the Stealth Station™ System Cranial Software biopsy depth gauge graphical display which presents during navigation in a cranial biopsy procedure. On June 9, 2021, a complaint was reported to Medtronic that during…
RecallHealth product recall | 2021-12-22
Cardinal Health has initiated a medical device correction for specific production lots of nonabsorbent towels with adhesives manufactured between March 2021 and October 2021 due to varying levels of adhesion. Affected non-absorbent towels are supplied in…
RecallHealth product recall | 2021-12-22
No stability data to support affected lots' shelf life.
RecallHealth product recall | 2021-12-22
Power wheelchairs with a LINX® Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile.
Recall start date: Nov 12, 2021
RecallHealth product recall | 2021-12-21