MEDLINE INDUSTRIES, LP - Northfield recall records

809 reported ongoing

822 records in this archive. Latest source date Jul 25, 2025.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

FDA device enforcement

Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270
FDA device enforcement

Medline Convenience kits used for various procedures: 1) CSTM PACEMAKER DRAPE PACK, Model Number: DYNJCD0339

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) CSTM PACEMAKER DRAPE PACK, Model Number:...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) UNIVERSAL DRAPE PACK, Model Number: DYNJCD0239

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) UNIVERSAL DRAPE PACK, Model Number: DYNJ...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ908337C

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ90...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) NEURO PACK WRO-LF, Model Number: DYNJ41856C; 2) STIM IMPLANT PACK, Model Number: DYNJ53032C; 3) WMC VP SHUNT PACK-LF, Mo...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) NEURO PACK WRO-LF, Model Number: DYNJ418...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number: DYNJ26971L; 2) VAGINAL DELIVERY PACK-LF, Model Number: DYNJ0378319P; 3) VUWC O...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B
FDA device enforcement

Medline Convenience kits used for various procedures: 1) STANDARD D&C, Model Number: DYNJ69733; 2) NHS - LAP BOWEL GNG, Model Number: DYNJ39904A; 3) LAPAROSCOPY GYN SURGERY PA, ...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) STANDARD D&C, Model Number: DYNJ69733; 2...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) ED CRASH C-SECTION TRAY, Model Number: MNS13635A; 2) C-SECTION PCH-LF, Model Number: DYNJ81281; 3) C-SECTION PACK-LF, Mo...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) ED CRASH C-SECTION TRAY, Model Number: M...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) PERI GYN PACK, Model Number: DYNJ80786; 2) D & C HYSTEROSCOPY PACK, Model Number: DYNJ21937J; 3) VAGINAL HYSTERECTOMY WR...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) PERI GYN PACK, Model Number: DYNJ80786; ...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK, Model Number: DYNJ68673; 2) D AND C PACK, Model Number: DYNJ66290A; 3) D & C PACK-LF, Model Number:...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) UTHET TYLER OB PACK, Model Number: DYNJ6...
FDA device enforcement

Medline Convenience kits used for various procedures: 1) BASIC CATARACT, Model Number: DYNJ41097A; 2) PK EYE, Model Number: DYNJ60631B; 3) CATARACT PACK, Model Number: DYNJ80316...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) BASIC CATARACT, Model Number: DYNJ41097A...
FDA device enforcement

Refer to RES

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Refer to RES
FDA device enforcement

Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: DYNJ40229A; 2) ARTHROSCOPY PACK-LF, Model Number: OPK382N; 3) ARTHROSCOPY NEW TE...

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Class IIReported ongoing

Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Official source for Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: ...
FDA device enforcement

Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C; 2) NEWBORN RESUSCITATION KIT, REF ACC010381A; 3) NEWBORN RESUSCITATION KIT, REF ACC0103...

Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.

Class IReported ongoing

Distribution: California

Official source for Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C; 2) NEWB...
FDA device enforcement

Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF

Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

Class IReported ongoing

Distribution: US: CA, FL, MN, NY, OH, OR, PA, TX, WV

Official source for Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEA...
FDA device enforcement

Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CPB ADJUNCT PACK, DR. C PACK, PK CUST CV A&B C CO, TOL DR R PACK, TOL DR. C PACK, T...

Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

Class IReported ongoing

Distribution: US: CA, FL, MN, NY, OH, OR, PA, TX, WV

Official source for Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CPB...
FDA device enforcement

Wayson Hydrocolloid Models: 1) Model Number: CUR5103, DBD-BNDG,WTRPRF,HYDRCLLD,CLR,2.36X3.93", 2) Model Number: MJ18004, DBD-MEIJER,BANDAGE,HYDROCOLLOID,HEEL,OVL 3) Model Number...

There is a potential for the sterility of the device to be compromised.

Class IIReported ongoing

Distribution: Worldwide Distribution: US (Nationwide) and OUS (Foreign) to countries of: Bermuda, Canada, Panama, Singapore

Official source for Wayson Hydrocolloid Models: 1) Model Number: CUR5103, DBD-BNDG,WTRPRF,HYDRCLLD,CLR,2.36X3.93", 2)...

Reasons in these listed records

  • There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
  • Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.
  • Medline medical procedure kits, containing Medtronic Aortic Root Cannula
  • Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

These examples come from this result page and are not a ranking of every recall reason.

Checking MEDLINE INDUSTRIES, LP - Northfield

Is there a recall on medline industries, lp - northfield right now?

This archive contains 822 records, including 809 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.

Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.

Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

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