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Displaying 1 - 15 of 2680 items.
Biomerieux identified a manufacturing event that may contribute to elevated rates of false negative results while using the Biofire RP2.1 panel. Biomerieux has not received any false negative complaints from the field but, out of an abundance of caution…
RecallHealth product recall | 2023-06-01
Affected lots are incorrectly labelled for use in the subpopulation that is less than 4 years of age.
RecallHealth product recall | 2023-06-01
Baxter Corporation is issuing an urgent medical device recall for the Allen Advance Chest Support to inform customers of the potential for the device to crack where the chest base and prone supports attach to the carbon fiber operating room (or) table…
RecallHealth product recall | 2023-06-01
Stryker has determined that size 11 (11mm) height peek Ogival Interbody Cage (OIC) was incorrectly laser marked as having a size 10 (10mm) height.
Recall start date: May 19, 2023
RecallHealth product recall | 2023-06-01
Currently, the Hemospray instructions for use states "Potential complications: when spraying in the retroflexed position, Hemospray powder may adhere to the outside of the endoscope. This may result in difficulty repositioning / removing the endoscope,…
RecallHealth product recall | 2023-05-31
The dextrose content is out of specification in the affected lot.
RecallHealth product recall | 2023-05-31
A concern with the software network binding of the Universal Copy Service (UCS), an ILMN proprietary software component present on ILMN instruments. The concern expressed was that the software process running as a tcp service was found to bind to…
RecallHealth product recall | 2023-05-31
Presence of Sorafenib in affected lots.
RecallHealth product recall | 2023-05-31
Health Canada advised that the Philaser Type 2.0 device is considered a class III medical device and requires a licence. The Philaser Type 2.0 device is not currently licensed, so we have stopped sales and advertisement of the Philaser Type 2.0…
RecallHealth product recall | 2023-05-31
Product sold without market authorization (DIN) in Canada.
RecallHealth product recall | 2023-05-30
This notice is to inform you that Bio-Rad Laboratories is initiating a recall due to a quality issue detected during an investigation into a positive agglutination test for the negative control serum provided in the Pastorex Toxo kit (cat #72724), for…
RecallHealth product recall | 2023-05-30
Bio-Rad Laboratories is initiating a recall due to a confirmed quality anomaly for Platelia aspergillus IgG test (cat #62783), for lot 2l0039 (expiry date: 2024/04/15). The current lot 2l0039 shows a decrease of Optical Density (OD) of all…
RecallHealth product recall | 2023-05-29
During extended operation of the MX40 with the PIC iX, the DHCP (dynamic host configuration protocol) lease can expire on the MX40. If the DHCP lease expires while the device is offline, upon reconnecting with the pic ix, a new IP address will be…
RecallHealth product recall | 2023-05-26
During an update of data used in a library shipped with Exoplan or made available on the download portal of Exocad, it was found that the use of a specific combination of an implant, sleeve and drill in a surgical kit can result in a hole being drilled…
RecallHealth product recall | 2023-05-25
Some of the tubes have no gel.
Recall start date: May 12, 2023
RecallHealth product recall | 2023-05-25