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Displaying 1 - 15 of 331 items.
Product sold without market authorization (DIN) Canada. Product contains undeclared pancreatin that is listed on the Prescription Drug List (provides more than 20 000 USP units of lipase activity/dose).
RecallHealth product recall | 2023-11-29
Affected lot may contain over-sized tablets.
RecallHealth product recall | 2023-11-27
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
Solution bags may be leaking in affected lots.
RecallHealth product recall | 2023-11-24
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
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