MEDLINE 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.
Read the official notice →- Date
- 2025-06-11
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU CDS983611N 3.…
- Classification
- Class I
- Units
- US distribution to CA, FL, IL, IN, KY, MA, MD, MN, NY, TX, VT, WA and WI. No…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2025-07-30
USMEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B;…
Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistributed domestically to California, Florida, Pennsylvania, and Texas. No…Official notice →- 2025-07-09
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV…
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the Catheter, the needle is slow…
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of IN, KY, CA, MI, TX, WA.Official notice → - 2025-07-02
- US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
There is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of VA.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.
- 2025-05-07
- US
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.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Panama and Canada.Official notice →
Other drugs & medical recalls in the United States
- 2025-06-11
- US
Mozarc Medical US LLC recalls Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Potential breach of sterile barrier packaging.
FDA · DeviceMozarc Medical US LLCWorldwide distribution - US Nationwide and the countries of Canada & Mexico.Official notice → - US
Flux Technology Inc. recalls Lazervida 10W diode laser cutter and engraver with Lazervida shield.
Lazervida 10W Diode Laser Engraver does not fully meet current Federal performance standards in certain areas. Specifically, the product does not incorporate the additional beam attenuator, remote interlock connector,…
- US
SunMed Holdings, LLC recalls Adult Manual Resuscitator with Medium Adult Mask, Bag REservoir, Filter, Manometer and 7 ft Oxygen Tubing, REF CPRM1116F
Affected lots were manufactured with B/V Filter incorrectly attached to the wrong port (patient port instead of the exhalation port). If not noticed prior to patient use, there would be interruption or delay in patient…
- US
Consumer Product Partners, LLC recalls Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc.,…
Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol
- US
Apotex Corp. recalls Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured…
Defective Container: This recall is being initiated due to a leaking unit stored horizontally.
- US
Torrent Pharma Inc. recalls Fluoxetine Tablets, USP, 20 mg, 28-count Carton (4x7 Unit-dose), Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA;…
CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.