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Displaying 1 - 15 of 220 items.
BD has identified internally that the infusion sets contain di(2-ethylhexyl) phthalate (DEHP) and have not been labeled accordingly.
Recall start date: November 13, 2023
RecallHealth product recall | 2023-11-23
In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…
RecallHealth product recall | 2023-11-17
The dissolution is out of specification in the affected lot.
RecallHealth product recall | 2023-11-16
Inadequate product labelling at point of sale (end product distributed in bulk form)
RecallHealth product recall | 2023-11-14
Per the VITROS CKMB slides instructions for use (IFU) "principles of the procedure" section, the spread layer of the CKMB slide contains goat antihuman CK-mm antibodies, which inhibit CK-mm (muscle) activity and ~50% of the CK-mb (heart) activity. The…
RecallHealth product recall | 2023-11-10
The manufacturer of the NIV angled mouthpiece with Notch 22F/15F, advised that devices in lots 32304444, 32305269 and 32306017 were produced with unintended open slits on the side of the mouthpiece body. This allows some of the respiratory gas to escape…
RecallHealth product recall | 2023-11-09
BD has identified internally that the infusion sets contain di(2-ethylhexyl) phthalate (DEHP) and have not been labeled accordingly.
Recall Start Date: October 12, 2023
RecallHealth product recall | 2023-11-09
Missing risk statement and indicated population on product label.
RecallHealth product recall | 2023-11-09
The impurity free salicylic acid is out of specification in the affected batches.
RecallHealth product recall | 2023-11-08
Presence of contamination in affected lot
RecallHealth product recall | 2023-11-08
The impurity free salicylic acid is out of specification in the affected batches.
RecallHealth product recall | 2023-11-08
In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…
RecallHealth product recall | 2023-11-07
Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iviewgt™ / xvi detector arms. when the detector arm is fully deployed there is no risk of uncontrolled…
RecallHealth product recall | 2023-11-07
Product imported and marketed without market authorization (DIN) in Canada.
RecallHealth product recall | 2023-11-03
Unomedical A/S has found that in rare cases the VariSoft infusion set connector detaches more easily from the infusion set than expected, requiring less force to disconnect than intended, thereby interrupting the delivery of insulin.
Recall start date…
RecallHealth product recall | 2023-11-01