MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP.…
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
Read the official notice →- Date
- 2025-02-26
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A,…
- Classification
- Class II
- Units
- US States: CA, NY
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 MEDLINE INDUSTRIES, LP - Northfield recalls
- 2025-03-26
USMEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) EYE PACK, Pack Number VAL038BSCLC
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide - US Nationwide and the country of Canada.Official notice →- US
MEDLINE INDUSTRIES, LP - Northfield recalls Proxima Drape labeled as PACK,BASIC,SIRUS,V,5/CS; PACK,BASIC IV,SIRUS,5/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,SET UP,NO…
Potential breach in pouch packaging which could lead to loss of sterility.
- US
- 2025-02-26
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397; medical procedure convenience kit
Medline is recalling medical convenience kits which were assembled with specific Coloplast Foley catheters and Prostatic catheters which were subsequently recalled due to a potential sterility issue detected during…
- 2025-02-05
- US
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ARTERIAL LINE PACK, REF DYNJ65208B, medical convenience kit containing Infusion Catheter with Antimicrobial Heparin…
Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT, Reorder number DYNDC3189; dressing change tray
Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the bioburden testing requirements of…
Other drugs & medical recalls in the United States
- 2025-02-26
- US
Augustine Temperature Management, LLC recalls Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode, 127 cm (50"), REF US502, to prevent or treat…
There is over-molding that stabilizes the connection between the cable and cable-entry on the mattress. It turns out that after about a year of use, the connector cable on the mattress can experience the same type of…
FDA · DeviceAugustine Temperature Management, LLCUS Nationwide distribution in the states of TX, AL, NV; AU, NZ.Official notice → - US
RAYSEARCH LABORATORIES AB recalls Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 1.0.0.951, 11.0.1.29,…
Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a HU-to-mass density CT…
FDA · DeviceRAYSEARCH LABORATORIES ABWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - US
Physio-Control, Inc. recalls LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF 11996-000515 Masimo¿…
Due to an error message that prevents users from utilizing carboxyhemoglobin saturation and methemoglobin saturation sensors on their monitor/defibrillator system.
FDA · DevicePhysio-Control, Inc.U.S. Nationwide distribution including in the states of CA, CO, CT, FL, GA,…Official notice → - US
Hollister Incorporated recalls AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
Hollister received reports of decreased skin barrier wear time which could can lead to tube migration
FDA · DeviceHollister IncorporatedWorldwide distribution - US Nationwide and the country of Canada.Official notice → - US
XTANT Medical Holdings, Inc recalls Irix-A Integrated Lumbar Fusion System, Model Number X080-423011-08PC (Spacer Assy, 42 X 30 X 8¿, 11mm, PC (STERILE)) and Model…
Certain implants in the Irix-A Lumbar Fusion System were distributed while labeled with an incorrect expiration date.
FDA · DeviceXTANT Medical Holdings, IncWorldwide - US Nationwide distribution in the states of AZ, CA, CO, LA, OH,…Official notice → - US
KCI USA, INC. recalls 3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit VIAKIT07S05/AU - V.A.C. VIA Starter Kit…
Due to increase in complaints related to leak alarms
FDA · DeviceKCI USA, INC.Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →