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
Read the official notice →- Date
- 2023-10-04
- Country
- United States
- Brand
- B. Braun Medical
- Product
- 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…
- Classification
- Class II
- Units
- US Nationwide distribution in the state of VA.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 B. Braun Medical recalls
- 2023-12-13
USB. Braun Medical, Inc. recalls Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump Set with Caresite Injection Site; 362032 15 drops/mL, priming…
In affected products, the tubing outer diameter may vary in size or the length of tubing may be too short. Both issues may lead to false air-in-line alarms, which will stop the infusion and interrupt therapy.…
- 2023-11-15
- US
B. Braun Medical, Inc. recalls TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV, Article No. 7S3070. Singapore only. IV injection set.
Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous…
FDA · DeviceB. Braun Medical, Inc.Worldwide distribution - US Nationwide and the countries of Canada and…Official notice → - 2023-11-01
- US
B. Braun Medical, Inc. recalls 8713051U, Infusomat Large Volume Pump, Wireless; Volumetric Infusion Pump System
Upstream occlusion alarm may sound when no occlusion exists, and the device will stop pumping. Interruption to the infusion of high-risk medications may lead to hemodynamic instability requiring medical intervention to…
FDA · DeviceB. Braun Medical, Inc.Domestic distribution nationwide. Foreign distribution to Canada.Official notice → - 2023-09-27
- US
B. Braun Medical, Inc. recalls Perifix¿ / Epidural anesthesia set, medicated
Product may be mislabeled with an incorrect lid stock label.
FDA · DeviceB. Braun Medical, Inc.US Distributions to states of - AR, AZ, CA, FL, GA, IL, MA, MO, NC, NJ, PA,…Official notice → - 2023-08-16
- US
B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018, NDC 0264-5802-00
Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.
- 2023-07-19
- US
B. Braun Medical Inc. recalls 0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container, Rx only, B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA, NDC…
Lack of assurance of sterility: bags have the potential to leak.
Other drugs & medical recalls in the United States
- 2023-10-04
- US
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…
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide distribution including in the states of…Official notice → - 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
Wolf, Henke Sass, Gmbh recalls Henke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneous, intracutaneous and intraarterial…
Sterile barrier might be damaged compromising the sterility of the device.
FDA · DeviceWolf, Henke Sass, GmbhWorldwide distribution - US Nationwide and the country of Canada.Official notice → - US
Waldemar Link GmbH & Co. KG (Mfg Site) recalls MobileLink Acetabular Cup System, Shell/Insert Adapter for Shell 74-80mm, Insert Size F, +12mm Offset 20 degrees…
Product is labeled with incorrect offset.
FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)Domestic distribution to AL, NJ, NV.Official notice → - US
3M Company - Health Care Business recalls 3M Attest Super Rapid Readout Biological Indicator, REF 1492V; used to qualify or monitor dynamic-air-removal steam…
Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid Readout Steam Challenge (1496V) may contain…
FDA · Device3M Company - Health Care BusinessWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →