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Regulatorische Updates

Regulatorische Entwicklungen von FDA, EMA, TGA und weltweit

#Health Canada ×

UPDATED
Regulatorische Updates
10. Sept. 2026•1 Min. Lesezeit
Stryker T2 Alpha IMN Advanced Locking Screw Lot Mislabelled, 75 mm Instead of 57.5 mm
Health Canada alerts that a Stryker T2 Alpha IMN advanced locking screw lot is mislabeled, containing 75 mm screws rather than the specified 57.5 mm.
UPDATED
Regulatorische Updates
4. Sept. 2026•1 Min. Lesezeit
Health Canada Alert: Stryker LifePak R35 Connector Seating Issue
Health Canada warns that certain printer and modem access port connectors on Stryker LifePak R35 monitor‑defibrillators may not be fully seated during production.
UPDATED
Regulatorische Updates
4. Sept. 2026•1 Min. Lesezeit
Boston Scientific Initiates Recall of Imager II Angiographic Catheters
Boston Scientific is recalling Imager II catheters due to reduced stabilizing agents in the tip, which may increase risk of tip degradation and detachment.
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UPDATED
Regulatorische Updates
4. Sept. 2026•1 Min. Lesezeit
Gore VIABAHN® Device Quality Issue Identified
Gore discovered some VIABAHN® devices were processed on equipment outside validated range, risking incorrect distal tip bonding.
UPDATED
Regulatorische Updates
31. Aug. 2026•1 Min. Lesezeit
Health Canada Recall: JAMP Temozolomide 140 mg Capsules Out of Specification
Health Canada has issued a retail recall of JAMP Temozolomide 140 mg capsules (lot RLTS0225A) because the active ingredient temozolomide is out of specification.
UPDATED
Regulatorische Updates
30. Aug. 2026•1 Min. Lesezeit
Unexpected Shutdown of Carestation 850 Anesthesia Systems When AC Power Is Lost
Health Canada alerts that Carestation 850 and 850C anesthesia systems may shut down unexpectedly if AC mains power is disconnected or lost.
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UPDATED
Regulatorische Updates
30. Aug. 2026•1 Min. Lesezeit
Health Canada issues alert on Pro+ model p7924a13 labeling error
The UDI label for model p7924a13 incorrectly lists a 40‑inch surface, while the approved configuration is a 36‑inch surface, risking incompatibility with bed frames.
UPDATED
Regulatorische Updates
29. Aug. 2026•1 Min. Lesezeit
Health Canada issues alert on KPC contamination in BIOFIRE FILMARRAY panels
Starting April 5 2026, Health Canada observed elevated KPC unexpected‑positive rates in final QC testing of BIOFIRE® FILMARRAY® Pneumonia, Pneumonia Plus and Joint Infection panels, linked to nucleic‑acid contamination in the pouch.
UPDATED
Regulatorische Updates
27. Aug. 2026•1 Min. Lesezeit
Health Canada Issues Alert on Maquet Percutaneous Insertion Kit Sterile Packaging
Health Canada reports failures in sterile barrier integrity testing for Maquet percutaneous insertion kits, limiting the FSCA to all PIK line products within shelf‑life.
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UPDATED
Regulatorische Updates
27. Aug. 2026•1 Min. Lesezeit
Health Canada Issues FSCA for Maquet PIK Line Packaging Integrity
Health Canada identified sterile barrier integrity failures in Maquet's percutaneous insertion kit and dilator sets, affecting all PIK line products within shelf-life.
UPDATED
Regulatorische Updates
26. Aug. 2026•1 Min. Lesezeit
Health Canada recalls Twins Herbal liquids Idakole and Pelorie for undeclared sildenafil
Health Canada has issued a recall of Twins Herbal’s Idakole and Pelorie liquid products, which were sold without market authorization and contain the undeclared prescription drug sildenafil. Consumers should stop use and contact a healthcare provider.
UPDATED
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
Beckman Coulter iQ200 and DxU 840m/850m Analyzers Report Fluid Leak Risk
Customer complaints revealed lamina fluid leaks in Beckman Coulter iQ200 and DxU 840m/850m analyzers due to a compromised rinse‑line check valve.