🔍 RecallPedia

Medline Convenience kits, labeled as: 1) BLOOD CULTURE COLLECTION KIT, Pack Number BP115; 2) NICU CNTRL LINE BLOOD DRAW KIT, Pack Number DYLAB1044; 3) NEURO ANGIO PACK, Pack Number DYNDA1431A; 4) BLOOD WITHDRAWAL KIT #2, Pack Number DYNDA1683A; 5) LCPH LAB DRAW KIT , Pack Number DYNDH1641A ; 6) LCPH LAB DRAW KIT , Pack Number DYNDH1641AH; 7) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798; 8) BLOOD CULTURE, Pack Number DYNDH1921; 9) BLOOD WITHDRAWAL TRAY, Pack Number DYNDV1588F; 10) BLOOD WITHDRAWAL TRAY , Pack Number DYNDV1588G ; 11) PHLEBECTOMY PK, Pack Number DYNJ84749; 12) ARTHROGRAPH TRAY, Pack Number MNS12670A; 13) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915; 14) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915H ; 15) LACERATION TRAY, Pack Number SUT20955

Class I - Dangerous
🏥 Medical Devices Recalled: April 8, 2024 MEDLINE INDUSTRIES, LP - Northfield Infusion Pumps

What Should You Do?

  1. Check if you have this product:
    BP115, Lot Number 21BBG338 ; BP115, Lot Number 21CBE353 ; BP115, Lot Number 21CBJ050 ; DYLAB1044, Lot Number 23GBM782 ; DYNDA1431A, Lot Number 2020012890; DYNDA1683A, Lot Number 2019011790; DYNDA1683A, Lot Number 2019032590; DYNDA1683A, Lot Number 2019042390; DYNDA1683A, Lot Number 2019072390; DYNDA1683A, Lot Number 2019090990; DYNDA1683A, Lot Number 2019102390; DYNDA1683A, Lot Number 2019112290; DYNDA1683A, Lot Number 2020030990; DYNDH1641A , Lot Number 21JBE248 ; DYNDH1641A , Lot Number 21JBY828 ; DYNDH1641AH, Lot Number 21JBE248 ; DYNDH1641AH, Lot Number 21JBY828 ; DYNDH1798, Lot Number 2022112990; DYNDH1921, Lot Number 23KBC196; DYNDV1588F, Lot Number 2019022090; DYNDV1588F, Lot Number 2019041890; DYNDV1588F, Lot Number 2019090390; DYNDV1588F, Lot Number 2020012890; DYNDV1588G , Lot Number 22GBL908 ; DYNDV1588G , Lot Number 22HBN586 ; DYNDV1588G , Lot Number 22JBI927 ; DYNDV1588G , Lot Number 22LBK218 ; DYNDV1588G , Lot Number 23ABJ940 ; DYNDV1588G , Lot Number 23EBB512 ; DYNDV1588G , Lot Number 23EBU397 ; DYNDV1588G , Lot Number 23IBU991 ; DYNDV1588G , Lot Number 23KBS797 ; DYNJ84749, Lot Number 23HBE651 ; DYNJ84749, Lot Number 23JBD780 ; MNS12670A, Lot Number 2022112990; MNS8915, Lot Number 21GBS360 ; MNS8915, Lot Number 21HBU417 ; MNS8915, Lot Number 21JBI844 ; MNS8915, Lot Number 21JBY844 ; MNS8915, Lot Number 21LBO003 ; MNS8915, Lot Number 21LBS501 ; MNS8915, Lot Number 22CBY070 ; MNS8915, Lot Number 22HBA169 ; MNS8915, Lot Number 22HBT299 ; MNS8915, Lot Number 22IBR400 ; MNS8915, Lot Number 22KBV233 ; MNS8915, Lot Number 23ABF223 ; MNS8915, Lot Number 23CBT546 ; MNS8915, Lot Number 23DBA141 ; MNS8915, Lot Number 23EBF405 ; MNS8915, Lot Number 23FBF145 ; MNS8915, Lot Number 23GBH740 ; MNS8915, Lot Number 23IBL050 ; MNS8915, Lot Number 23JBK017 ; MNS8915, Lot Number 23LBE535 ; MNS8915, Lot Number 24ABQ710 ; MNS8915H , Lot Number 21GBS360 ; MNS8915H , Lot Number 21HBU417 ; MNS8915H , Lot Number 21JBI844 ; MNS8915H , Lot Number 21JBY844 ; MNS8915H , Lot Number 21LBO003 ; MNS8915H , Lot Number 21LBS501 ; MNS8915H , Lot Number 22CBY070 ; MNS8915H , Lot Number 22HBA169 ; MNS8915H , Lot Number 22HBT299 ; MNS8915H , Lot Number 22IBR400 ; MNS8915H , Lot Number 22KBV233 ; MNS8915H , Lot Number 23ABF223 ; MNS8915H , Lot Number 23CBT546 ; MNS8915H , Lot Number 23DBA141 ; MNS8915H , Lot Number 23EBF405 ; MNS8915H , Lot Number 23FBF145 ; MNS8915H , Lot Number 23GBH740 ; MNS8915H , Lot Number 23IBL050 ; MNS8915H , Lot Number 23JBK017 ; MNS8915H , Lot Number 23LBE535 ; MNS8915H , Lot Number 24ABQ710 ; SUT20955, Lot Number 2020012890
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
MEDLINE INDUSTRIES, LP - Northfield
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Medline Convenience kits, labeled as: 1) BLOOD CULTURE COLLECTION KIT, Pack Number BP115; 2) NICU CNTRL LINE BLOOD DRAW KIT, Pack Number DYLAB1044; 3) NEURO ANGIO PACK, Pack Number DYNDA1431A; 4) BLOOD WITHDRAWAL KIT #2, Pack Number DYNDA1683A; 5) LCPH LAB DRAW KIT , Pack Number DYNDH1641A ; 6) LCPH LAB DRAW KIT , Pack Number DYNDH1641AH; 7) INFUSION CENTER BLOOD DRAW KIT, Pack Number DYNDH1798; 8) BLOOD CULTURE, Pack Number DYNDH1921; 9) BLOOD WITHDRAWAL TRAY, Pack Number DYNDV1588F; 10) BLOOD WITHDRAWAL TRAY , Pack Number DYNDV1588G ; 11) PHLEBECTOMY PK, Pack Number DYNJ84749; 12) ARTHROGRAPH TRAY, Pack Number MNS12670A; 13) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915; 14) BLOOD CULTURE COLLECTION KIT, Pack Number MNS8915H ; 15) LACERATION TRAY, Pack Number SUT20955

Product Codes/Lot Numbers:

BP115, Lot Number 21BBG338 ; BP115, Lot Number 21CBE353 ; BP115, Lot Number 21CBJ050 ; DYLAB1044, Lot Number 23GBM782 ; DYNDA1431A, Lot Number 2020012890; DYNDA1683A, Lot Number 2019011790; DYNDA1683A, Lot Number 2019032590; DYNDA1683A, Lot Number 2019042390; DYNDA1683A, Lot Number 2019072390; DYNDA1683A, Lot Number 2019090990; DYNDA1683A, Lot Number 2019102390; DYNDA1683A, Lot Number 2019112290; DYNDA1683A, Lot Number 2020030990; DYNDH1641A , Lot Number 21JBE248 ; DYNDH1641A , Lot Number 21JBY828 ; DYNDH1641AH, Lot Number 21JBE248 ; DYNDH1641AH, Lot Number 21JBY828 ; DYNDH1798, Lot Number 2022112990; DYNDH1921, Lot Number 23KBC196; DYNDV1588F, Lot Number 2019022090; DYNDV1588F, Lot Number 2019041890; DYNDV1588F, Lot Number 2019090390; DYNDV1588F, Lot Number 2020012890; DYNDV1588G , Lot Number 22GBL908 ; DYNDV1588G , Lot Number 22HBN586 ; DYNDV1588G , Lot Number 22JBI927 ; DYNDV1588G , Lot Number 22LBK218 ; DYNDV1588G , Lot Number 23ABJ940 ; DYNDV1588G , Lot Number 23EBB512 ; DYNDV1588G , Lot Number 23EBU397 ; DYNDV1588G , Lot Number 23IBU991 ; DYNDV1588G , Lot Number 23KBS797 ; DYNJ84749, Lot Number 23HBE651 ; DYNJ84749, Lot Number 23JBD780 ; MNS12670A, Lot Number 2022112990; MNS8915, Lot Number 21GBS360 ; MNS8915, Lot Number 21HBU417 ; MNS8915, Lot Number 21JBI844 ; MNS8915, Lot Number 21JBY844 ; MNS8915, Lot Number 21LBO003 ; MNS8915, Lot Number 21LBS501 ; MNS8915, Lot Number 22CBY070 ; MNS8915, Lot Number 22HBA169 ; MNS8915, Lot Number 22HBT299 ; MNS8915, Lot Number 22IBR400 ; MNS8915, Lot Number 22KBV233 ; MNS8915, Lot Number 23ABF223 ; MNS8915, Lot Number 23CBT546 ; MNS8915, Lot Number 23DBA141 ; MNS8915, Lot Number 23EBF405 ; MNS8915, Lot Number 23FBF145 ; MNS8915, Lot Number 23GBH740 ; MNS8915, Lot Number 23IBL050 ; MNS8915, Lot Number 23JBK017 ; MNS8915, Lot Number 23LBE535 ; MNS8915, Lot Number 24ABQ710 ; MNS8915H , Lot Number 21GBS360 ; MNS8915H , Lot Number 21HBU417 ; MNS8915H , Lot Number 21JBI844 ; MNS8915H , Lot Number 21JBY844 ; MNS8915H , Lot Number 21LBO003 ; MNS8915H , Lot Number 21LBS501 ; MNS8915H , Lot Number 22CBY070 ; MNS8915H , Lot Number 22HBA169 ; MNS8915H , Lot Number 22HBT299 ; MNS8915H , Lot Number 22IBR400 ; MNS8915H , Lot Number 22KBV233 ; MNS8915H , Lot Number 23ABF223 ; MNS8915H , Lot Number 23CBT546 ; MNS8915H , Lot Number 23DBA141 ; MNS8915H , Lot Number 23EBF405 ; MNS8915H , Lot Number 23FBF145 ; MNS8915H , Lot Number 23GBH740 ; MNS8915H , Lot Number 23IBL050 ; MNS8915H , Lot Number 23JBK017 ; MNS8915H , Lot Number 23LBE535 ; MNS8915H , Lot Number 24ABQ710 ; SUT20955, Lot Number 2020012890

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3059-2024

Related Recalls

Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A; 3. INTUBATION TRAY, Kit Number ACC010392; 4. INTUBATION KIT, Kit Number ACC010467A; 5. ADULT AIRWAY TRAY, Kit Number ACC010469; 6. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480; 7. TRAY 2 INTUBATION DRAWER, Kit Number ACC010480A; 8. ADULT INTUBATION, Kit Number ACC010540; 9. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593A; 10. DIFFICULT AIRWAY TRAY #1, Kit Number ACC010593B; 11. INTUBATION TRAY, Kit Number DYNDA1847A; 12. INTUBATION TRAY (ADULT), Kit Number DYNJAA245A.

MEDLINE INDUSTRIES, LP - Northfield

Class I - Dangerous

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.

Jul 25, 2025 Other Medical Devices View Details →

Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C; 2. DRAWER 5 - POSITION 3, Kit Number ACC010532; 3. DRAWER #4C ADULT, Kit Number ACC010671; 4. DRAWER #2, Kit Number ACC010728.

MEDLINE INDUSTRIES, LP - Northfield

Class I - Dangerous

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to the failure of the light to illuminate as intended.

Jul 25, 2025 Other Medical Devices View Details →