PlainRecalls
FDA Devices Verify with FDA Devices → Moderate Class II Ongoing

Medline Convenience kits, labeled as: 1) SINGLE SHOT EPIDURAL PACK-LF, Pack Number DYNJ0708470K ; 2) EPIDURAL CSTM PACK-LF , Pack Number DYNJ0844004; 3) CUSTOM EPIDURAL PACK-LF , Pack Number DYNJ0934752F ; 4) EPIDURAL PACK-LF, Pack Number DYNJ0957053D ; 5) EPIDURAL PACK-LF, Pack Number DYNJ0957053DH; 6) SINGLE SHOT TRAY, Pack Number DYNJ32736; 7) CONTINUOUS EPIDURAL TRAY-LF , Pack Number DYNJ34352A ; 8) SINGLE SHOT EPIDURAL-LF , Pack Number DYNJ36046A ; 9) PHOENIXVILLE EPIDURAL TRAY, P

Reported: September 18, 2024 Initiated: April 8, 2024 #Z-2987-2024

MEDLINE INDUSTRIES, LP - Northfield issued this FDA Devices recall on September 18, 2024. Classified as Moderate severity (Class II). The recall was issued because: Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, bre…. This recall notice is sourced from official FDA Devices enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This FDA Devices action (record #Z-2987-2024) was formally reported on September 18, 2024, with the manufacturer initiating the action on April 8, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. MEDLINE INDUSTRIES, LP - Northfield is listed as the recalling firm, operating out of Northfield, IL. The number of affected units is not disclosed in the agency filing, which is common for drug and food recalls where lot-level tracking supersedes unit counts.

The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Worldwide distribution.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 2 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

Unknown

Related Recalls

6

6 from same agency

Product Description

Medline Convenience kits, labeled as: 1) SINGLE SHOT EPIDURAL PACK-LF, Pack Number DYNJ0708470K ; 2) EPIDURAL CSTM PACK-LF , Pack Number DYNJ0844004; 3) CUSTOM EPIDURAL PACK-LF , Pack Number DYNJ0934752F ; 4) EPIDURAL PACK-LF, Pack Number DYNJ0957053D ; 5) EPIDURAL PACK-LF, Pack Number DYNJ0957053DH; 6) SINGLE SHOT TRAY, Pack Number DYNJ32736; 7) CONTINUOUS EPIDURAL TRAY-LF , Pack Number DYNJ34352A ; 8) SINGLE SHOT EPIDURAL-LF , Pack Number DYNJ36046A ; 9) PHOENIXVILLE EPIDURAL TRAY, Pack Number DYNJ40991A ; 10) UNIVERSAL SCOPE PACK, Pack Number DYNJ45052A ; 11) SPINAL PACK , Pack Number DYNJ48916B ; 12) PUH SPINAL BLOCK TRAY , Pack Number DYNJ49205B ; 13) EPIDURAL PACK , Pack Number DYNJ50772A ; 14) TRANSFORAMINAL PACK , Pack Number DYNJC3420D ; 15) EPIDURAL PREP TRAY-LF , Pack Number DYNJRA0135B; 16) SUPPORT TRAY-LF, Pack Number DYNJRA0198; 17) SPINAL TRAY W/GERTIE MARX NDL , Pack Number DYNJRA0245 ; 18) EPIDURAL TRAY , Pack Number DYNJRA0260 ; 19) SPINAL EPIDURAL (TUOHY) PF, Pack Number DYNJRA0270B; 20) EPIDURAL TRAY-LF, Pack Number DYNJRA0275A; 21) SPINAL BLOCK TRAY- LF , Pack Number DYNJRA0413B; 22) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number DYNJRA0506A; 23) EPIDURAL TRAY , Pack Number DYNJRA0508 ; 24) SPINAL TRAY W/GERTIE MARX NDL , Pack Number DYNJRA0555 ; 25) COMBINED SPINAL/EPIDURAL PACK , Pack Number DYNJRA0635 ; 26) SPINAL BLOCK, 25G QUINCKE , Pack Number DYNJRA0766 ; 27) TRANSFORAMINAL 22X5PF , Pack Number DYNJRA0777F; 28) TRANSFORMINAL TRAY, Pack Number DYNJRA0822A; 29) SPINAL TRAY, Pack Number DYNJRA0836A; 30) SPINAL TRAY , Pack Number DYNJRA0978A; 31) UNIVERSAL BLOCK TRAY, Pack Number DYNJRA0988 ; 32) TRAY, SPINAL, WHIT 24GX4, Pack Number DYNJRA1034 ; 33) TRANSFORAMINAL TRAY , Pack Number DYNJRA1730A; 34) SPINAL BLOCK 25G WHTCRE 5S BU , Pack Number DYNJRA9028 ; 35) SPINAL BLOCK 25G WHTCRE 5S BU , Pack Number DYNJRA9028H; 36) TRAY, SPINAL PENCIL POINT 25G , Pack Number DYNJRA9030 ; 37) SPINAL BLOCK TRAY, 22G QUINCKE, Pack Number DYNJRA9036 ; 38) SPINAL BLOCK TRAY, 22G QUINCKE, Pack Number DYNJRA9036H; 39) SPINAL BLOCK, 25G QUINCKE , Pack Number DYNJRA9037 ; 40) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0012 ; 41) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0024D; 42) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0055A; 43) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0058D; 44) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0078C; 45) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0082D; 46) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0111C; 47) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0133 ; 48) COMPLETE SINGLE SHOT TRAY , Pack Number PAIN0136A; 49) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0146C; 50) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0157G; 51) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0171C; 52) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0191I; 53) NORTON SINGLE SHOT EPIDURAL , Pack Number PAIN0215A; 54) EPIDURAL TRAY , Pack Number PAIN0225 ; 55) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0242B; 56) SINGLE SHOT EPIDURAL-LF , Pack Number PAIN0250A; 57) SINGLE SHOT EPIDURAL-LF , Pack Number PAIN0256B; 58) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0261A; 59) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0262A; 60) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0265C; 61) EPI TRAY, SINGLE , 20G-LF , Pack Number PAIN0274A; 62) EPI TRAY CONTI 17G TUOHY, Pack Number PAIN0275 ; 63) EPIDURAL TRAY-LF, Pack Number PAIN0279C; 64) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0280C; 65) SINGLE DOSE EPI-LF, Pack Number PAIN0300B; 66) SINGLE DOSE EPIDURAL TRAY-LF, Pack Number PAIN0317A; 67) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0334A; 68) EPIDURAL TRAY-LF, Pack Number PAIN0349B; 69) SINGLE DOSE EPIDURAL TRAY-LF, Pack Number PAIN0357B; 70) SHOT EPIDURAL TRAY-LF , Pack Number PAIN0362 ; 71) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0386B; 72) CONTINUOUS EPIDURAL TRAY, Pack Number PAIN0390 ; 73) SINGLE SHOT EPIDURAL T

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.

Details

Distribution
Worldwide distribution.
Location
Northfield, IL

Recall Profile

Structured summary of the FDA Devices recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Ongoing
Recall number Z-2987-2024
Date reported September 18, 2024
Date initiated April 8, 2024
Recalling firm MEDLINE INDUSTRIES, LP - Northfield
Units affected Not disclosed
Distribution Worldwide distribution.

Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.

Frequently Asked Questions

What product was recalled? ▼
Medline Convenience kits, labeled as: 1) SINGLE SHOT EPIDURAL PACK-LF, Pack Number DYNJ0708470K ; 2) EPIDURAL CSTM PACK-LF , Pack Number DYNJ0844004; 3) CUSTOM EPIDURAL PACK-LF , Pack Number DYNJ0934752F ; 4) EPIDURAL PACK-LF, Pack Number DYNJ0957053D ; 5) EPIDURAL PACK-LF, Pack Number DYNJ0957053DH; 6) SINGLE SHOT TRAY, Pack Number DYNJ32736; 7) CONTINUOUS EPIDURAL TRAY-LF , Pack Number DYNJ34352A ; 8) SINGLE SHOT EPIDURAL-LF , Pack Number DYNJ36046A ; 9) PHOENIXVILLE EPIDURAL TRAY, Pack Number DYNJ40991A ; 10) UNIVERSAL SCOPE PACK, Pack Number DYNJ45052A ; 11) SPINAL PACK , Pack Number DYNJ48916B ; 12) PUH SPINAL BLOCK TRAY , Pack Number DYNJ49205B ; 13) EPIDURAL PACK , Pack Number DYNJ50772A ; 14) TRANSFORAMINAL PACK , Pack Number DYNJC3420D ; 15) EPIDURAL PREP TRAY-LF , Pack Number DYNJRA0135B; 16) SUPPORT TRAY-LF, Pack Number DYNJRA0198; 17) SPINAL TRAY W/GERTIE MARX NDL , Pack Number DYNJRA0245 ; 18) EPIDURAL TRAY , Pack Number DYNJRA0260 ; 19) SPINAL EPIDURAL (TUOHY) PF, Pack Number DYNJRA0270B; 20) EPIDURAL TRAY-LF, Pack Number DYNJRA0275A; 21) SPINAL BLOCK TRAY- LF , Pack Number DYNJRA0413B; 22) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number DYNJRA0506A; 23) EPIDURAL TRAY , Pack Number DYNJRA0508 ; 24) SPINAL TRAY W/GERTIE MARX NDL , Pack Number DYNJRA0555 ; 25) COMBINED SPINAL/EPIDURAL PACK , Pack Number DYNJRA0635 ; 26) SPINAL BLOCK, 25G QUINCKE , Pack Number DYNJRA0766 ; 27) TRANSFORAMINAL 22X5PF , Pack Number DYNJRA0777F; 28) TRANSFORMINAL TRAY, Pack Number DYNJRA0822A; 29) SPINAL TRAY, Pack Number DYNJRA0836A; 30) SPINAL TRAY , Pack Number DYNJRA0978A; 31) UNIVERSAL BLOCK TRAY, Pack Number DYNJRA0988 ; 32) TRAY, SPINAL, WHIT 24GX4, Pack Number DYNJRA1034 ; 33) TRANSFORAMINAL TRAY , Pack Number DYNJRA1730A; 34) SPINAL BLOCK 25G WHTCRE 5S BU , Pack Number DYNJRA9028 ; 35) SPINAL BLOCK 25G WHTCRE 5S BU , Pack Number DYNJRA9028H; 36) TRAY, SPINAL PENCIL POINT 25G , Pack Number DYNJRA9030 ; 37) SPINAL BLOCK TRAY, 22G QUINCKE, Pack Number DYNJRA9036 ; 38) SPINAL BLOCK TRAY, 22G QUINCKE, Pack Number DYNJRA9036H; 39) SPINAL BLOCK, 25G QUINCKE , Pack Number DYNJRA9037 ; 40) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0012 ; 41) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0024D; 42) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0055A; 43) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0058D; 44) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0078C; 45) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0082D; 46) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0111C; 47) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0133 ; 48) COMPLETE SINGLE SHOT TRAY , Pack Number PAIN0136A; 49) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0146C; 50) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0157G; 51) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0171C; 52) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0191I; 53) NORTON SINGLE SHOT EPIDURAL , Pack Number PAIN0215A; 54) EPIDURAL TRAY , Pack Number PAIN0225 ; 55) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0242B; 56) SINGLE SHOT EPIDURAL-LF , Pack Number PAIN0250A; 57) SINGLE SHOT EPIDURAL-LF , Pack Number PAIN0256B; 58) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0261A; 59) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0262A; 60) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0265C; 61) EPI TRAY, SINGLE , 20G-LF , Pack Number PAIN0274A; 62) EPI TRAY CONTI 17G TUOHY, Pack Number PAIN0275 ; 63) EPIDURAL TRAY-LF, Pack Number PAIN0279C; 64) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0280C; 65) SINGLE DOSE EPI-LF, Pack Number PAIN0300B; 66) SINGLE DOSE EPIDURAL TRAY-LF, Pack Number PAIN0317A; 67) SINGLE SHOT EPIDURAL TRAY-LF, Pack Number PAIN0334A; 68) EPIDURAL TRAY-LF, Pack Number PAIN0349B; 69) SINGLE DOSE EPIDURAL TRAY-LF, Pack Number PAIN0357B; 70) SHOT EPIDURAL TRAY-LF , Pack Number PAIN0362 ; 71) SINGLE SHOT EPIDURAL TRAY , Pack Number PAIN0386B; 72) CONTINUOUS EPIDURAL TRAY, Pack Number PAIN0390 ; 73) SINGLE SHOT EPIDURAL T. Recalled by MEDLINE INDUSTRIES, LP - Northfield.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 18, 2024. Severity: Moderate. Recall number: Z-2987-2024.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2987-2024) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

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Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Read our methodology — how this data is sourced, computed, and verified.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).