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MEDLINE INDUSTRIES, LP - Northfield Recalls

822 recalls on record · December 29, 2021 to October 1, 2025 · Drugs, Medical Devices

Recalls by year

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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

December 4, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STER
Hazard: The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
December 4, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268B; 2) COMBINED SPINAL AND
Hazard: The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
December 4, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
Hazard: The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos. DYNJ04049 (cases), DYNJ04049H (eaches)
Hazard: Tip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls URINE KIT W/BD CUP, SKU DYLAB1001A; Component No. 503581
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls URINE KIT, SKU DYKM1845; Component No. 503581
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls URINE COLLECTION VHC, SKU DYLAB1016; Component No. 503581
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls URINE COLLECTION KIT, SKU DYKM1848A DYKM2005 DYKM2151 DYLAB1004 DYLAB1004A DYLAB1006 DYLAB1012 ; Component No. 50
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls URINALYSIS KIT 4, SKU DYLAB1021; Component No. 503581
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls UA KIT, SKU DYKM1690A; Component No. 503581
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Lab Kit, SKU DYLAB1018; Component No. 503581
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Clean Catch Kit, SKU DYKM1833A; Component No. 503581
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C
Hazard: 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.
November 20, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A
Hazard: 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.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline EYE PACK, REF LYN036EPESB; medical procedure convenience kit
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: 1) NEW LONDON TOTAL KNEE CDS, REF CDS982519W; 2) HAND
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: 1) EYE PACK, REF DYNJ19492L; 2) PHACO PACK, REF DYNJ223
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: a) OB PACK-LF, REF DYNJ0912449M; b) OB PACK, REF DYNJ
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: a) ABDOMINAL HYSTERECTOMY TEGH-LF, REF DYNJ46730; b)
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: a) LITHOTOMY PACK, REF DYNJ24362C; b) MAJOR GYNE LAPA
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: 1) L&D/OB PACK-LF, REF DYNJ0213264O; 2) VAG DELIVERY HL
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: a) NEURO PACK, REF DYNJ37909A; b) SHUNT PACK, REF DYN
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline AMBULATORY MINI PACK, REF DYNJ82579; medical procedure convenience kit
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: a) UNIVERSAL DRAPE PACK, REF DYNJ44114; b) DRAPE PACK
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline TUBAL LIGATION PACK, REF DYNJ66230B; medical procedure convenience kit
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline PEDIATRIC DRAPE PK, REF DYNJ81297; medical procedure convenience kit
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline IV TEAM PICC, REF DYNJ48222; medical procedure convenience kit
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline CHEST TUBE INSERTION TRAY ADUL, REF CHT1165; medical procedure convenience kit
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: 1) THORACENTESIS TRAY, REF 00-400616J; 2) HH PACK SONICAT
Hazard: XXX
October 30, 2024Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline brand medical procedure convenience kits, labeled as: a) PLASTIC PACK, REF DYNJ42735A; b) DR SELEM PACK, RE
Hazard: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.