Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion Pumps, Product code 3570009.
There is the potential for reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of…
Read the official notice →- Date
- 2022-02-09
- Country
- United States
- Brand
- Baxter Healthcare
- Product
- Baxter Spectrum IQ Infusion Pumps, Product code 3570009.
- Classification
- Class I
- Units
- Worldwide Distribution. US nationwide Puerto Rico and St. Thomas. There was…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-04-27
US
Baxter Healthcare Corporation recalls Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Product is mislabeled as self-righting Luer slip tip caps, yellow.
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide distribution in the states of FL, GA,…Official notice →- 2022-04-06
US
Baxter Healthcare Corporation recalls MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S, R5C4482, R5C4483, R5C4484
Devices distributed lacked regulatory clearance.
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of California, Colorado, District of…Official notice →US
Baxter Healthcare Corporation recalls Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.
An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use.
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide distribution in the states of AK, AZ,…Official notice →- 2022-03-30
US
Baxter Healthcare Corporation recalls Compella Therapy Air Supply Unit
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →- 2022-02-16
US
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, REF R5C4482E
Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as…
- 2021-11-17
US
Baxter Healthcare Corporation recalls Hemodialysis Delivery System, Software Version 2.x.
If the operator initiates therapy with a saved prescription profile and makes a change to the prescription after a disposable filter change using the Same Patient button, the system may suggest values from the original…
FDA · DeviceBaxter Healthcare CorporationDistributed nationwide to AL, AR, AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KY,…Official notice →
Other drugs & medical recalls in the United States
- 2022-02-09
US
DIXI MEDICAL USA recalls The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or Electrode ) is a smooth electrode that is 0.8 mm in diameter…
Potential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
US
XTANT Medical recalls X060-0270, 8mm Titanium Insert, Axle Interspinous Fusion System.
The proximal opening of the inserts exhibit an out of specification condition which would prevent the crossbar plates from appropriately engaging with the insert.
US
LivaNova USA, Inc. recalls Vagus Nerve Stimulation (VNS) Therapy Leads, PerenniaDURA, Model: 303. Model 303-20 PereniaDURA Lead (2.0 mm electrode inner diameter) and…
A manufacturing issue may cause the silicone tubing wall thickness of vagus nerve stimulation leads to be less than the design specification. If the tubing becomes completely breached, the patient may experience…
US
Empowered Diagnostics LLC recalls CovClear COVID-19 Rapid Antigen Test, ATG 900-031
COVID test kits were offered for sale and distributed to consumers in the United States without marketing approval, clearance, or authorization from FDA.
US
US
Teva Pharmaceuticals USA recalls Tretinoin Capsules, 10 mg, 100 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0555-0808-02
Failed Dissolution Specifications; Low Out of specification (OOS) results for dissolution.