MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON…
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Read the official notice →- Date
- 2024-12-04
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON EPID 20G NYL…
- Classification
- Class II
- Units
- US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2024-12-11
USMEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE convenience kits labeled as: PORT INSERTION PACK, REF DYNJ81597
Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.
- 2024-12-04
- US
MEDLINE INDUSTRIES, LP - Northfield recalls ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use…
Identified lots of Olympus product may be missing sterile and manufacturing lot numbers and expiration dates on the sterile packaging. The information can be found on the outer box or zipper bag label. Medline is…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of NY.Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls (1) Medline Pacer Implant Pack, REF DYNJ59194A, 4 kits/case, sterile; and (2) Medline Thoracotomy Morristown, REF…
Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AL, GA, MA, NJ, and PA.Official notice → - 2024-11-20
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos. DYNJ04049 (cases), DYNJ04049H (eaches)
Tip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distributions in the states of AL, AR, CO, CT, FL, IA, IN, KS,…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Lab Kit, SKU DYLAB1018; Component No. 503581
Specimen container included in kits is labeled as sterile, but has been identified to be non-sterile. Long-term consequences may include unnecessary treatment and/or prolonged hospitalization.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AL, CA, FL, GA, IL, KY, MO, MS,…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A
Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of TN.Official notice →
Other drugs & medical recalls in the United States
- 2024-12-04
- US
MicroSurgical Technology Inc recalls Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps and Scissors)…
Due to pin coming off of handles.
FDA · DeviceMicroSurgical Technology IncU.S.: CT, GA, MN, MT and TX. O.U.S.: Netherlands 24 total devices = 6 devices…Official notice → - US
GE Medical Systems, LLC recalls SIGNA Architect AIR, Nuclear Magnetic Resonance Imaging System
Gradient coils for certain MR systems (see affected product list in this letter), under specific conditions, can produce elevated acoustic noise during scanning.
FDA · DeviceGE Medical Systems, LLCWorldwide Distribution: US (nationwide) and OUS (foreign) to countries of:…Official notice → - US
Smith & Nephew Medical, Ltd. recalls RENASYS EDGE The RENASYS¿ EDGE pump is indicated for patients who would benefit from a suction pump (NPWT), as it may promote wound…
Due to issues with battery depletion and inability to recharge if the batteries are not appropriately maintained.
FDA · DeviceSmith & Nephew Medical, Ltd.U.S.: AL, CA, CO, FL, HI, IN, KY, NE, NY, PA, SC, TN and WI O.U.S.: CanadaOfficial notice → - US
KCI USA, INC. recalls V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an integrated wound…
Due to potential system error alarm and the inability to initiate therapy as a result of broken occlusion sensors.
FDA · DeviceKCI USA, INC.Worldwide Distribution: U.S.(nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, FL,…Official notice → - US
Defibtech, LLC recalls Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View…
Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could…
- US
Defibtech, LLC recalls Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on…
Within the Irish Market, a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could lead…