MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: T AND A PACK -LF, REF DYNJ85792
It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.
Read the official notice →- Date
- 2025-05-07
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Medline procedure kits, labeled as: T AND A PACK -LF, REF DYNJ85792
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Panama and Canada.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2025-06-11
USMEDLINE INDUSTRIES, LP - Northfield recalls Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU…
Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS distribution to CA, FL, IL, IN, KY, MA, MD, MN, NY, TX, VT, WA and WI. No…Official notice →- 2025-05-21
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Three is the potential for the retractors to puncture through the sterile packaging.
- 2025-05-14
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits, Model Number 750830
A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was inadvertently stored in Medline warehouses at temperatures outside of the labeled storage requirements.
- 2025-04-23
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) NAIL PACK, Model Number: SUT15830A;
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Canada, Mexico,…Official notice → - 2025-04-16
- US
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT, Model Number: MJ18004V2; 2) MJ BANDAGE HYDROCOLLOID…
There is a potential for the sterility of the device to be compromised.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of:…Official notice →
Other drugs & medical recalls in the United States
- 2025-05-14
- US
FDC Limited recalls Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 10mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad,…
Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
- US
- 2025-05-07
- US
Olympus Corporation of the Americas recalls Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro SuperPulsed Laser System Model/Catalog Numbers:…
Preset treatment parameters are not consistently being used in accordance with the IFU.
FDA · DeviceOlympus Corporation of the AmericasWorldwide distribution - US Nationwide and the countries of AU, CA, SG, DE,…Official notice → - US
Medtronic Neuromodulation recalls Enhanced Verify Evaluation Handset (CFN HH90130FA)
Evaluation handsets may not be able to communicate with the neurostimulator due to handsets having a faster processing speed than prior handsets. An inability to connect may cause the therapy to stop being delivered…
FDA · DeviceMedtronic NeuromodulationUS Nationwide distribution including in the states of AR, AZ, CA, CO, CT, FL,…Official notice → - US
IBA Dosimetry GmbH recalls myQA iON; Article Number: MQ10-000;
Wrong analysis results can occur if the user creates two structures with the same name, except for one differing by a special character.
FDA · DeviceIBA Dosimetry GmbHWorldwide - US Nationwide distribution in the states of AL, AR, FL, GA, KS,…Official notice → - US
Waldemar Link GmbH & Co. KG (Mfg Site) recalls Posterior Femoral Augment; Item Numbers: (1) 880-310/11 (Sz. 0 - cemented sm), (2) 880-310/21 (Sz. 0 - cemented lg), (3)…
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)US Nationwide distribution in the states of AL, AZ, CA, CO, FL, GA, IN, IL,…Official notice →