MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedural kits labeled as: ARTHROGRAPH TRAY, Pack Number MNS12670A
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.
Read the official notice →- Date
- 2024-09-04
- Country
- United States
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Product
- Medline procedural kits labeled as: ARTHROGRAPH TRAY, Pack Number MNS12670A
- Classification
- Class II
- Units
- Worldwide
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2024-09-18
US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider, Nano-Coated, Compatible w/ FT10 37 cm FT10 SW…
Potential for an incomplete seal on the packaging tray.
US
MEDLINE INDUSTRIES, LP - Northfield recalls CRANIOTOMY PACK, Pack Number DYNJ46552O
A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed. In the event that the user assumes…
US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits, labeled as: 1) SUTURING SET PACK ASSY P791011, Pack Number 59112; 2) SUTURE SET, 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.
- 2024-08-28
US
MEDLINE INDUSTRIES, LP - Northfield recalls LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar,…Official notice →- 2024-08-14
US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) NEPHROLOGY PACK, Pack Number DYNJ59089; 2) NERVE BLOCK TRAY, Pack Number DYNJRA1221A
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 OUS countries of: AE, AI, BB, CA,…Official notice →- 2024-07-10
US
MEDLINE INDUSTRIES, LP - Northfield recalls Sterile convenience kits: a. Medline Retrograde PK-22025203-LF, Pack #DYNJ47873K, containing a Pure Pouch containing…
Surgical convenience kits containing Pure Pouch component that has weak seals which may result in a breach in sterility of the contents if the seal fails.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AL, CA, CO, CT, FL, IL, IN, MD,…Official notice →
Other drugs & medical recalls in the United States
- 2024-09-04
US
Cypress Medical Products LLC recalls McKesson Syringe 60CC, Luer Lock Tip, Sterile, ITEM NO 102-S60C. Model No. 102-S60C - SYRINGE, LL 60CC (25/BX 4BX/CS)
Affected syringes lack FDA clearance.
FDA · DeviceCypress Medical Products LLCUS distribution only. Domestic distribution nationwide.Official notice →US
Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001113;
Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure…
US
US
Agfa N.V. recalls DR 800. Digital Radiography X-ray System.
Potential for the front lever chain of the DR 800 table to fail.
FDA · DeviceAgfa N.V.Worldwide - US Nationwide distribution in the states of CA, FL, IL, IN, KS,…Official notice →US
RONAN MEDICAL LLC recalls BrainFeedback Pro 2 Device - is intended as an instrument that provides a visual and auditory signal corresponding to the status of a…
Neurofeedback systems removed due to missing design and development documentation and devices may not perform as intended.
FDA · DeviceRONAN MEDICAL LLCWorldwide - US Nationwide distribution in the states of CA, FL, TN, MI, IL, CT…Official notice →US
Abbott Diagnostics Technologies AS recalls Afinion 2 Analyzer, model #1116986, US refurbished, CLIA waived.
Five Afinion 2 (AF2) Analyzer were incorrectly market configured as Moderate Complexity and distributed to customers. Use of moderately complex assays by waived laboratories could result in erroneous results.
FDA · DeviceAbbott Diagnostics Technologies ASUS Nationwide distribution in the states of AZ, IN, MA, MN, and OH.Official notice →