MEDLINE INDUSTRIES, LP - Northfield recalls Namic FLUID DELIVERY SET, REF 91300040
Products have a lack of sterility assurance.
Read the official notice →- Date
- 2024-05-22
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Namic FLUID DELIVERY SET, REF 91300040
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AL, FL, KY, MS, TX, WA, WI, NC,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2024-06-12
USMEDLINE INDUSTRIES, LP - Northfield recalls Syringes labeled as: a) SYR 10ML L/L CONTROL, Item Numbers: 1. DNSC91881, 2. DYNJSYRPPC10; b) SYRINGE 20ML BLUE L/L LOW PR,…
These syringes were identified to be 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 countries of Canada, Panama.Official notice →- 2024-06-05
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, labeled as follows: a) PARACERVICAL PUD TRAY, REF DYNDH1832; b) AHS PARACERVICAL/PUDENDAL…
Trumpet Needle Guide ring can detach when excessive pressure is applied.
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) REF DYNJ18860, Polyurethane Cuff 6.0 mm ID; (2) REF…
Complaints have been received that the device inflation tube detached and/or tore from the main tube, resulting in potential moisture buildup, loss of pressure, or inability to inflate. There were also reports the…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistribution was nationwide. There was government/military distributon.…Official notice → - 2024-04-17
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS
Medline is recalling certain lots of our Adult Portable Bed Rails that were manufactured after the mandatory compliance requirement (ASTM F3186-17, Standard Specification for Adult Portable Bed Rails and Related…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the country of Canada.Official notice → - 2024-04-10
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Blood Pressure Unit, Model (REF) Numbers: a) MDS4001, b) MDS4001LA, c) MDS4001PLUS
The firm provided a set of specifications for the device, but some units of the device were manufactured non-compliant with the specifications. However, the firms Receiving Dept. accepted these units into inventory
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion manual surgical kits labeled as: a) STERILE 4-1/2" S/S SCISSOR (SS5031), Product Code 65145; b) STERILE S/B…
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Panama, Canada.Official notice →
Other drugs & medical recalls in the United States
- 2024-05-22
- US
Baxter Healthcare Corporation recalls Spectrum IQ Infusion pump, Product Code 357009
There is a potential for cracks on the mount of the front panel of the device.
FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of Ohio, Wisconsin.Official notice → - US
Karl Storz Endoscopy recalls LASER Application Instrument, 23 cm, REF: 8694; LEUNIG-GREVERS LASER Application, REF: 461000
Laser surgical instruments have no specific evidence of a validated reprocessing method, therefore these instruments lack sterility assurance, so once the instruments have gone through reprocessing after use and then…
FDA · DeviceKarl Storz EndoscopyWorldwide distribution - US Nationwide in the states of OH, CA, FL, MA, TX,…Official notice → - US
Wishbone Medical, Inc. recalls WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant as the packaging and part number indicated.
FDA · DeviceWishbone Medical, Inc.US distribution to Florida, New Jersey and Connecticut.Official notice → - US
- US
TriMed Inc. recalls TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref:…
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
FDA · DeviceTriMed Inc.US Nationwide distribution in the states of AK, AR, AZ, CA, FL, HI, IL, LA,…Official notice → - US
Ossur H / F recalls RKN130002, RHEO KNEE 2 YR WARRANTY, MD, CE, External lower limb prosthetic component
Due to firmware issues with the prosthetic knee, there is the potential for unintended warnings and device shutdown which could result in patient falls.
FDA · DeviceOssur H / FUS Nationwide distribution in the states of AL, AZ, CA, CO, DE, FL, GA, HI,…Official notice →