Baxter Healthcare Corporation recalls NaviCare Nurse Call/Voalte Nurse Call
An issue has been identified with Phillips (Emergin) and Longleaf non relay (Connexall, Vocera, Cerner) wireless integrations used with NaviCare/Voalte Nurse Call, software versions 3.9.100 through 3.9.300. Calls…
Read the official notice →- Date
- 2022-07-06
- Country
- United States
- Brand
- Baxter Healthcare
- Product
- NaviCare Nurse Call/Voalte Nurse Call
- Classification
- Class II
- Units
- nationwide and Canada
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-08-24
US
Baxter Healthcare Corporation recalls Acetaminophen Injection, 10 mg/mL, 1,000 mg/100 mL, 100 mL VIAFLO container bag, Single Dose Container, For Intravenous Use Only,…
Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.
- 2022-08-03
US
Baxter Healthcare Corporation recalls ABACUS TPN (Total Parenteral Nutrition) Calculation software, Product codes: 8300-0167 (Abacus V3.1 CE), 8300-0168 (Abacus V3.1…
There is a potential risk of medication error when using specific Abacus Order Entry & Calculation software.
FDA · DeviceBaxter Healthcare CorporationUnited States (including Puerto Rico), Argentina, Bermuda, Chile, Colombia,…Official notice →- 2022-07-27
US
Baxter Healthcare Corporation recalls Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of…
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →- 2022-07-06
US
Baxter Healthcare Corporation recalls #1 MAC F/O LARYNGOSCOPE; F/O Laryngoscope Set-MAC; F/O Laryngoscope Set-MAC W/LED
Packaging error.
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the countries of Japan, Canada,…Official notice →- 2022-06-08
US
Baxter Healthcare Corporation recalls 3,65 m Extension Set with Luer-lock Connector
Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of CA, MO, MA, AZ, TX, FL, NY, MD, OH.Official notice →US
Baxter Healthcare Corporation recalls In-Line ventilator adaptor
There is a potential of reduced oxygenation or pneumothorax/barotrauma to occur when the Volara system is used with in-line ventilator in home care environment.
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of TX, FL, VA, KY, CA, AZ, WI, IL,…Official notice →
Other drugs & medical recalls in the United States
- 2022-07-06
US
Skytron, Div. The KMW Group, Inc recalls Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
Under certain circumstances, the mounting screws may loosen or pull out from the attachment point on the Ergon 3 boom when the GCX Channel Mounting Accessory was used with the VST clamp as a monitor mount on the boom.
FDA · DeviceSkytron, Div. The KMW Group, IncWorldwide distribution - US Nationwide and the countries of Canada and Japan.Official notice →US
Getinge Usa Sales Inc recalls VOLISTA StandOP Surgical Light, Product Code/Part Numbers ARD568811901 VLT600SF AIM STP ARD568811911 VLT600SF AIM STP ARD568811961…
Paint particles may detach and fall in the operating field. In the worst case scenario, infection, organ irritation, hypersensitivity reaction, and tissue granuloma may result if paint particles fall during surgical…
FDA · DeviceGetinge Usa Sales IncWorldwide distribution - US Nationwide distribution in the states of AR, AZ,…Official notice →US
K2M, Inc. recalls Yukon Straight Rod 4.0 x120mm; Cat# 7601-540120. Used to provide immobilization and stabilization of spinal segments.
Some of the rods in this lot were observed to have discoloration, later confirmed to be indication of trace amounts of inorganic phosphorous compound. This may produce a mild irritating or inflammatory response;…
FDA · DeviceK2M, Inc.Domestic distribution to FL GA NE NV NY OH OK SC Foreign distribution to…Official notice →US
Davol, Inc. recalls HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Cojoined Suction and Irrigation Tubing,…
The product is not able to provide irrigation.
FDA · DeviceDavol, Inc.Worldwide distribution - US Nationwide and the country of Canada.Official notice →US
Fresenius Medical Care Holdings, Inc. recalls Optiflux 200NRe Dialyzer Finished Assy., Model no. 0500320E
Dialyzers were distributed after being exposed to cold temperatures which exceeded the low-temperature range in the firm's standard operating procedure.
FDA · DeviceFresenius Medical Care Holdings, Inc.US Nationwide distribution in the state of Pennsylvania.Official notice →US
Volcano Corp recalls Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797
Digital IVUS catheter instructions for use ( IFU) do not contain contrainidications
FDA · DeviceVolcano CorpWorldwide distribution - US Nationwide distribution in the states of NY, CA,…Official notice →