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FDA
December 20, 2024
Lidl Recalls Taste of Deutschland Buttered Vegetables Due to Undeclared Milk Allergens
DECEMBER 20, 2024 – Lidl US is recalling all lots of their Taste of Deutschland Buttered Vegetables 10.5 oz box…
FDA
December 20, 2024
Recall of Jose Madrid Salsa Chipotle Con Queso
Jose Madrid Salsa is announcing a voluntary recall of our Chipotle Con Queso Salsa. The salsa is being recalled because…
FDA
December 20, 2024
Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With Plum 360, A+, and A+3 Infusion Systems Due to Reports of Allegedly Counterfeit, Untested Batteries In Use
Some CSB batteries intended for use with Plum 360, A+ or A+3 infusion pumps may be counterfeit and are not…
FDA
December 20, 2024
Early Alert: Nephroscope Sheath Issue from Trokamed GmbH
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
FDA
December 20, 2024
Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution (EPINEPHrine Nasal Solution, USP) Due to the Potential for Administration Errors
Endo, Inc (OTCQX: NDOI) (“Endo”), announced today that one of its operating subsidiaries, Endo USA, Inc., is voluntarily recalling all…
FDA
December 19, 2024
Orgain Issues Voluntary Allergy Alert on Possible Undeclared Peanut Residue in a Single Batch of 30G Protein Organic Plant Based Powder – Chocolate 2.01lb
Orgain of Irvine, California is voluntarily recalling a single batch of its 30g Protein Organic Plant Based Powder – Chocolate…
FDA
December 18, 2024
Hologic, Inc. Recalls BioZorb Marker Due to Complications with Implanted Devices
Hologic, Inc. is recalling BioZorb Marker due to complications and adverse events with implanted devices.
FDA
December 18, 2024
Implantable Marker Recall: Hologic Removes BioZorb 3D Bioabsorbable Markers due to Risk for Patient Complications
BioZorb Markers are implantable and used to mark soft tissue for procedures. They are being recalled after reports of patient…
FDA
December 18, 2024
Update: Do Not Use BioZorb Marker Implantable Radiographic Marker Devices: FDA Safety Communication
The FDA’s updated information about BioZorb Marker.
FDA
December 18, 2024
Catheter Correction: Boston Scientific Updates Use Instructions for POLARx and POLARx FIT Cryoablation Balloon Catheters due to Higher than Anticipated Number of Reports of Atrio-Esophageal Fistula
POLARx Cryoablation Balloon Catheters treat atrial fibrillation. After reports of atrio-esophageal fistula, the use instructions are being updated.
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