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Last updated: June 2022
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Last updated: 2022
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Displaying 1 - 15 of 62 items.
Product sold without market authorization. Affected lots are labelled with unauthorized claims.
RecallHealth product recall | 2022-06-30
The sterility is out of specification in the affected lot (Periodic Media Fill Validation failure).
RecallHealth product recall | 2022-06-30
UPDATE: June 29, 2022
There continues to be a national shortage of specialized infant formulas for infants with food allergies and certain medical conditions. This includes extensively hydrolyzed formulas and amino acid-based formulas. There is no…
AlertPublic advisory | 2022-06-29
Zimmer GmbH is conducting a medical device field safety corrective action (removal) for one lot of the NCB femoral screws. The product in scope is part of a mix-up with a NCB humeral screw that differs in dimensions and therefore it has been decided to…
RecallHealth product recall | 2022-06-27
Abbott is notifying customers of the potential for programmer software (Merlin pcs) and remote monitoring software applications (Merlin.net) to display overestimated predicted battery longevity for certain pacemakers. Pacemaker/battery functionality,…
RecallHealth product recall | 2022-06-27
Voluntary recall-interim order authorization not approved.
Recall start date: December 2, 2021
RecallHealth product recall | 2022-06-27
Voluntary recall-interim order authorisation not approved.
Recall start date: December 2, 2021
RecallHealth product recall | 2022-06-27
Voluntary recall- interim order authorisation not approved.
Recall start date: December 2, 2021
RecallHealth product recall | 2022-06-27
In rare cases, when the device is switched on directly in defibrillator mode, cancellations of heart rhythm analysis after 30 seconds have been reported.
Recall start date: June 17, 2022
RecallHealth product recall | 2022-06-27
On June 14, 2022, the manufacturer Fresenius Medical Care Ag & Co. Kgaa notified Fresenius Medical Care Canada, Inc. that during regular quality inspections of Aquac Uno H devices, it was discovered that the internal ethernet cable had not been…
RecallHealth product recall | 2022-06-27
During internal product/process review (April 2022), it was discovered that there is a potential for the core diameter to be undersized, which may lead to the router breaking. To date, Stryker has not been made aware of any adverse events related to this…
RecallHealth product recall | 2022-06-27
1. Difficulty separating stylet from needle, which could result in inadvertent removal of the entire needle assembly or inability to remove the stylet from an indwelling intraosseous needle, both resulting in functional loss of intraosseous access. 2.…
RecallHealth product recall | 2022-06-27
The Benzalkonium Chloride assay is out of specification in the affected lot.
RecallHealth product recall | 2022-06-23
The dissolution for vitamin D3 is out of specification in the affected lot.
RecallHealth product recall | 2022-06-22
The products may contain undeclared ingredients which are listed on the Prescription Drug List.
RecallHealth product recall | 2022-06-21