Avanos Medical, Inc. recalls MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL
The External Retention Bolster contained in the kit may be a larger diameter than the tube.
Read the official notice →- Date
- 2022-02-16
- Country
- United States
- Brand
- Avanos Medical
- Product
- MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Canada and Chile.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Avanos Medical recalls
- 2023-06-14
USAvanos Medical, Inc. recalls AVNS ambIT System - PIB/PCA W 2.5in Cath, Product Code: 220509
Some of the ambIT kits were potentially distributed without an air in-line filter.
FDA · DeviceAvanos Medical, Inc.Worldwide distribution - US Nationwide distribution in the states of Texas and…Official notice →- 2023-04-26
- US
Avanos Medical, Inc. recalls Avanos Ballard Oral Care Swab, Bulk Packed, Product Codes: a) 12241, b) 12243, c) 12251
Incorrect expiration date.
FDA · DeviceAvanos Medical, Inc.Worldwide distribution - US Nationwide and the countries of Canada, Germany,…Official notice → - 2023-03-22
- US
Avanos Medical, Inc. recalls BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics, Elbow Manifold.
Potential for product manifold to crack during use on patients, possibly causing leaks in the respiratory circuit and can lead to the patient receiving inadequate ventilation.
FDA · DeviceAvanos Medical, Inc.US Nationwide distribution in the state of Oklahoma.Official notice → - 2022-11-16
- US
Avanos Medical, Inc. recalls Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: SUMMIT MEDICAL…
Sterile extension sets were distributed without an expiration date
- 2022-05-25
- US
Avanos Medical, Inc. recalls Avanos Cortrak 2 Enteral Access System (EAS)
Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol.
FDA · DeviceAvanos Medical, Inc.Worldwide Distribution. US Nationwide, Australia, Austria, Canada, Germany,…Official notice → - 2022-04-06
- US
Avanos Medical, Inc. recalls BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use
Product was distributed with incorrect expiration date.
FDA · DeviceAvanos Medical, Inc.Worldwide distribution - US Nationwide distribution in the states of Oklahoma…Official notice →
Other drugs & medical recalls in the United States
- 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…
- US
R82 A/S recalls R82 by ETAC Push Brace for High-Low
The chrome surface of the push brace can crack during use, potentially cutting the user.
FDA · DeviceR82 A/SWorldwide distribution - US Nationwide distribution in the states of North…Official notice → - US
Mallinckrodt Pharmaceuticals Ireland Ltd recalls THERAKOS CELLEX Photopheresis Procedural Kit, CLXUSA
This recall was initiated to recover a Dunnage Case, which is a case of three (3) CLXUSA kits. This Dunnage Case was shipped on 02-Dec-2021. Dunnage is used during the sterilization process and is not intended for…
FDA · DeviceMallinckrodt Pharmaceuticals Ireland LtdUS Nationwide distribution in the states of CA, FL, GA, MA, MI, NC, NJ, NY,…Official notice → - US
E25Bio, Inc. recalls E25Bio COVID-19 Direct Antigen Rapid Test ; E25Bio COVID-19 DART Kit
The Test is not authorized, cleared, or approved by FDA for clinical diagnostic or screening purposes. It was distributed without sufficient directions or controls in place.
FDA · DeviceE25Bio, Inc.US Nationwide distribution in the states of MA, FL, and HI.Official notice → - US
Argon Medical Devices, Inc recalls 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
Guidewire included with two lots of Arterial Line Kits would not fit through the needle of the same kit. This could potentially lead to a slight delay in the procedure and minor blood loss.
FDA · DeviceArgon Medical Devices, IncUS Nationwide distribution in the states of AL, CA, DE, IL, IN, LA, MT, NV,…Official notice → - US
Fresenius Medical Care Holdings, Inc. recalls Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)- Indicated for long-term (> 6 hours)…
Error messages 206 (yellow) and 208 (red) technical failure, flow measurement during use of the Novalung System imply that the communication between flow sensor and sensor box is interrupted. An interrupted…
FDA · DeviceFresenius Medical Care Holdings, Inc.US Nationwide distribution in the states of AL, AZ, CA, CO, FL, IL, MI, NJ,…Official notice →