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BioMérieux Inc. Recalls VITEK 2 AST Kit due to Incorrect Ceftriaxone Concentrations
Monday, April 29, 2024 11:00:00 PM CST
BioMérieux is recalling their VITEK 2 AST cards, used for testing bacterial sensitivity to antibiotics, due to excessive Ceftriaxone in two wells.
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2024 Medical Device Recalls
Monday, April 29, 2024 11:00:00 PM CST
2024 Medical Device Recalls
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SonarMed Inc. Recalls Airway Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty
Sunday, April 28, 2024 11:00:00 PM CST
SonarMed Airway acoustic sensors recalled due to a restricted inner diameter resulting in difficulty passing a suction catheter through the sensor.
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SonarMed Inc. Recalls Airway Monitors Due to a Software Anomaly Resulting in Failure to Detect a Partial Obstruction in 2.5mm Sensors and Up To 3mm Distal to the Sensor Tip
Sunday, April 28, 2024 11:00:00 PM CST
SonarMed Airway monitors recalled for a software issue where it fails to detect partial obstructions in 2.5mm sensors and within 3mm of sensor tip.
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FDA Encourages the Public to Follow Established Choking Rescue Protocols: FDA Safety Communication
Thursday, April 25, 2024 11:00:00 PM CST
These choking rescue protocols include abdominal thrusts (also called the “Heimlich” maneuver) for children and adults but not anti-choking devices.
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Elekta Instrument AB Recalls Disposable Biopsy Needle Kit for Leksell Stereotactic System for Possibly Containing Microscopic Stainless Steel Debris on the Inside of the Biopsy Needle
Thursday, April 25, 2024 11:00:00 PM CST
Elekta recalls Disposable Biopsy Needles (911933) from batch 837838839 due to potential microscopic stainless steel debris inside.
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Draeger, Inc. Recalls Perseus A500 Anesthesia System for Risk of Sudden Unexpected Shutdown When Used on Battery Power
Wednesday, April 24, 2024 11:00:00 PM CST
The Perseus A500 that provides anesthesia and/or ventilation during surgical or diagnostic procedures may unexpectedly shutdown while using battery power.
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Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and Stay-Safe/Luer Lock Adapter for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBA
Wednesday, April 24, 2024 11:00:00 PM CST
Fresenius Stay-Safe Catheter Extension Sets and Stay-Safe/Luer Lock Adapter may expose patients who weigh less than 40 kg to higher than allowable levels of NDL-PCBA.
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UPDATE: Evaluating Plastic Syringes Made in China for Potential Device Failures: FDA Safety Communication
Wednesday, April 24, 2024 11:00:00 PM CST
UPDATE: Evaluating Plastic Syringes Made in China for Potential Device Failures: FDA Safety Communication
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Update: Potential Risk of Exposure to Toxic Compounds When Using Hemodialysis and Peritoneal Dialysis Systems – Letter to Health Care Providers
Wednesday, April 24, 2024 11:00:00 PM CST
The FDA expanded its evaluation of the potential risk of exposure to toxic compounds when using hemodialysis and peritoneal dialysis systems
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InfuTronix, LLC Recalls Nimbus and Nimbus II Infusion Pump Systems for Multiple Device Failures That May Cause Severe Injury and Death
Wednesday, April 24, 2024 11:00:00 PM CST
Nimbus and Nimbus II infusion pumps may experience one or more issues that can cause severe patient injury and death.
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Outset Medical, Inc. Recalls Certain Tablo Hemodialysis Systems for Risk of Patient Exposure to Higher Than Allowable Levels of Toxic Compound NDL-PCBAs
Wednesday, April 24, 2024 11:00:00 PM CST
The Tablo Hemodialysis System may expose patients to higher than allowable levels of NDL-PCBAs.
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Avoiding Drug Interactions
People often combine foods. For example, chocolate and peanut butter might be considered a tasty combination. But eating chocolate and taking certain drugs might carry risks. In fact, eating chocolate and taking monoamine oxidase...
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