MEDLINE INDUSTRIES, LP - Northfield recalls namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS,ST. *,…
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Read the official notice →- Date
- 2025-04-02
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS,ST. *, REF 60010511;…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of The Netherlands,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2025-04-16
US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC…
Medline medical procedure kits, containing Medtronic Aortic Root Cannula
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS: CA, FL, MN, NY, OH, OR, PA, TX, WVOfficial notice →- 2025-04-02
US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters, Medline Item Numbers: 401582R, 401904R, 401904R,…
Devices may have higher than expected amounts of bacterial endotoxin.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AR, AZ, CA, CO, IA, IL, KS, OR,…Official notice →US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number…
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 distribution - US Nationwide and the country of Canada.Official notice →- 2025-03-26
US
MEDLINE 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
Other drugs & medical recalls in the United States
- 2025-04-02
US
Merit Medical Systems, Inc. recalls Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D
Hydrophilic Sheath Introducer labeled for 4F dilators may instead incorrectly contain 5F dilators. Incorrect dilator use may result in procedure delay.
FDA · DeviceMerit Medical Systems, Inc.International distribution to the country of Japan.Official notice →US
Zimmer, Inc. recalls NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model Number 00-5962-042-10
The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label does not match with the compatibility statements "USE WITH PLATE 5, 6" in the translations section of the same label.
FDA · DeviceZimmer, Inc.Worldwide - US Nationwide distribution in the states pf CA, KS, MA, MD, ME,…Official notice →US
Orthofix U.S. LLC recalls Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device, sterile, implant grade titanium alloy: (1) REF 82-3300SP,…
The product is mislabeled with the incorrect anterior height of 10mm, but the laser marking on the implant and corresponding trial both show the correct anterior height of 10.5mm.
FDA · DeviceOrthofix U.S. LLCUS Nationwide distribution in the states of California, Colorado, and Missouri.Official notice →US
St. Jude Medical recalls CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web Application Model…
Due to issues associated with data migration of patient information and results to a Cloud service, the firm has received complaint associated with some patient profile information being duplicated while other patient…
FDA · DeviceSt. Jude MedicalU.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA,…Official notice →US
US
Baxter Healthcare Corporation recalls Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to…
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of AR, CA, FL, IA, IN, LA, MO, MT,…Official notice →