Baxter Healthcare Corporation recalls Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.
Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical Device Correction for the Cardio Server E3 ECG Management System software listed below due to a report of the caliper tool becoming…
Read the official notice →- Date
- 2023-10-04
- Country
- United States
- Brand
- Baxter Healthcare
- Product
- Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide distribution including in the states of…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Baxter Healthcare recalls
- 2023-11-15
US
Baxter Healthcare Corporation recalls Novum IQ Syringe infusion system, Product Code 40800BAXUS
Baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms, the pump may display an Infusion Complete alarm even though…
FDA · DeviceBaxter Healthcare CorporationUS Nationwide Distribution to states of: AR, AZ, CA, FL, GA, HI, IA, IN, KS,…Official notice →- 2023-11-08
US
Baxter Healthcare Corporation recalls HILLROM PROGRESSA+ BED, Product Codes: P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033, P7501A000052,…
Progressa+ beds have the potential for static buildup from the casters and/or power drive. This static electricity could be passed to the operator through the transport handle during transport, resulting in a mild…
FDA · DeviceBaxter Healthcare CorporationUS Nationwide Distribution in the states of: CA, FL, IN, MA, NY, OH, TX, VAOfficial notice →- 2023-10-25
US
Baxter Healthcare Corporation recalls Doxil (doxorubicin hydrochloride liposome injection) 50 mg in 25 mL (2 mg/mL), Single-Dose Vial, Rx only, Manufactured for: Baxter…
CGMP Deviations: Product was exposed to temperatures exceeding the labeled storage conditions during transportation were released by mistake.
- 2023-09-20
US
Baxter Healthcare Corporation recalls Welch Allyn Connex Spot Monitor
Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the state of CA.Official notice →- 2023-09-06
US
Baxter Healthcare Corporation recalls Dianeal PD-2 Peritonial Dialysis Solution with 1.5% Dextrose, 5000 mL AMBU-FLEX ll Container with yellow pull ring, Rx Only, Baxter…
Lack of Assurance of Sterility: Potential presence of leaks originating from the Luer component.
- 2023-08-30
US
Baxter Healthcare Corporation recalls Bendamustine HCl Injection, 100mg/4mL (25mg/mL), One 4 mL Multiple-Dose Vial, Rx only, Manufactured for Baxter Healthcare…
Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.
Other drugs & medical recalls in the United States
- 2023-10-11
US
Dr. Berne's Whole Health Products recalls Dr. Berne's Organic Castor Oil Eye Drops, Net WT 30 mL/1 fl oz bottle, Distributed by: Dr. Berne's Whole Health Products,…
CGMP Deviations
FDA · DrugDr. Berne's Whole Health ProductsNationwide and UK, Canada, Italy, India, Australia, Germany, Switzerland,…Official notice →US
- 2023-10-05
US
CURiO Recalls Capri Blue Pet Products Due to Risk of Exposure to Bacteria (Recall Alert)
The recalled pet products can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are…
- 2023-10-04
US
CareFusion 303, Inc. recalls BD Pyxis MedBank MedPass Software, REF: 139088-01
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to…
US
Stryker Corporation recalls Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462
Expired Product distributed
FDA · DeviceStryker CorporationUS Nationwide distribution in the states of NY, NC, GA, TN, KY, IL, UT, AZ,…Official notice →US
B. Braun Medical, Inc. recalls B.Braun NORM-JECT Luer Lock Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid…
The sterile blister packaging may be damaged, and sterility may be compromised