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FDA Devices Verify with FDA Devices → Moderate Class II Ongoing

Medline Convenience kits labeled as: 1) CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036O; 2) CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036OH; 3) CATH ACCESSORY PACK, Pack Number 0M-CP31433J; 4) 3" RADIAL ARTERIAL LINE KIT- OR, Pack Number ART1210; 5) PERF. ASSOC. CUT DOWN TRAY, Pack Number BM17BAD; 6) CATHETER ADD A CATH TRAY, Pack Number CVI4970; 7) BIOPSY TRAY, Pack Number DYNDH1129; 8) ARTHROGRAM TRAY, Pack Number DYNDH1134; 9) BRISTOL MYELOGRAM, Pack Number DYNDH1228; 10) LU

Reported: September 18, 2024 Initiated: April 8, 2024 #Z-2993-2024

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-2993-2024) 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) CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036O; 2) CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036OH; 3) CATH ACCESSORY PACK, Pack Number 0M-CP31433J; 4) 3" RADIAL ARTERIAL LINE KIT- OR, Pack Number ART1210; 5) PERF. ASSOC. CUT DOWN TRAY, Pack Number BM17BAD; 6) CATHETER ADD A CATH TRAY, Pack Number CVI4970; 7) BIOPSY TRAY, Pack Number DYNDH1129; 8) ARTHROGRAM TRAY, Pack Number DYNDH1134; 9) BRISTOL MYELOGRAM, Pack Number DYNDH1228; 10) LUMBAR TRAY, Pack Number DYNDH1540A; 11) RADIOLOGY BASIC PACK, Pack Number DYNDH1827; 12) BLOOD CULTURE KIT W/BOTTLES, Pack Number DYNDH1932; 13) BIOPSY PACK, Pack Number DYNDL1462B; 14) CATH LAB PACK-LF, Pack Number DYNJ0105963Q; 15) CARDIAC CATH HARPER PACK-LF, Pack Number DYNJ0161912G; 16) CATH LAB PACK-LF, Pack Number DYNJ0173400P; 17) CATH LAB PACK-LF, Pack Number DYNJ0194968AG; 18) PICC LINE PACK-LF, Pack Number DYNJ0275614F; 19) PEDI CATH PACK-LF, Pack Number DYNJ0429201L; 20) SPECIAL PROCEDURE ANGIO PACK, Pack Number DYNJ04386U; 21) RADIOLOGY PACK, Pack Number DYNJ04562S; 22) IR PACK, Pack Number DYNJ04674U; 23) IR PACK, Pack Number DYNJ04674UH; 24) LEFT HEART PACK-LF, Pack Number DYNJ0490280PH; 25) LT HEART/ANGIOGRAPHY PACK-LF, Pack Number DYNJ0537652AG; 26) SM CARDIAC CATH PACK-LF , Pack Number DYNJ0621195TH; 27) CATH LAB PACK-LF, Pack Number DYNJ0755738R; 28) CARDIAC CATH PACK-LF, Pack Number DYNJ0781476AAH ; 29) CARDIAC CATH PACK-LF, Pack Number DYNJ0781918NH; 30) CATH LAB PACK , Pack Number DYNJ07919GH; 31) PACEMAKER PACK-LF , Pack Number DYNJ0830939ACH ; 32) CARDIAC CATH PACK-LF, Pack Number DYNJ0843627G ; 33) PICC INSERTION PACK-LF, Pack Number DYNJ0880659D; 34) PEDS HEART CATH PACK-LF, Pack Number DYNJ0897998D; 35) RADIAL ARTERY CATH PACK-LF, Pack Number DYNJ0945414BH; 36) RADIAL ARTERY CATH PACK-LF, Pack Number DYNJ0945414CH; 37) CATH LAB PACK , Pack Number DYNJ10117JH; 38) CARDIAC CATH PACK, Pack Number DYNJ17081S; 39) DEPAUL ANGIO PROCEDURE PACK, Pack Number DYNJ19937I; 40) PV/PTA TRAY-RF, Pack Number DYNJ21944VH; 41) ANGIO TRAY, Pack Number DYNJ23438M; 42) ANGIO TRAY, Pack Number DYNJ23438N; 43) ANGIO TRAY, Pack Number DYNJ23438O; 44) ADULT CARDIAC CATH PACK, Pack Number DYNJ23455Q; 45) VIR PACK, Pack Number DYNJ23499MH; 46) HEART CATH-SMH, Pack Number DYNJ24483FH; 47) CATH LAB PACK , Pack Number DYNJ24802PH; 48) ANGIO DRAPE PACK, Pack Number DYNJ24806KH; 49) RADIOLOGY STD TRAY, Pack Number DYNJ25029RH; 50) CARDIAC CATH PACK, Pack Number DYNJ26305N; 51) DIAGNOSTIC ADULT-LF , Pack Number DYNJ27239DH; 52) HEART CATH LT PACK, Pack Number DYNJ31282I; 53) ANGIO PACK, Pack Number DYNJ31339I; 54) CARDIAC CATH PACK, Pack Number DYNJ31847I; 55) NEURO ANGIO TRAY-LF, Pack Number DYNJ34882M; 56) HEART CATH II PACK CHS-LF, Pack Number DYNJ35605M; 57) ISSAQUA CATH/IR PACK, Pack Number DYNJ36738G; 58) PEDS CARDIAC PACK, Pack Number DYNJ37418MH; 59) SPECIAL PROCEDURE PACK-LF, Pack Number DYNJ38050F; 60) SPECIAL PROCEDURE PACK-LF, Pack Number DYNJ38050FH; 61) SPECIAL PROCEDURE PACK, Pack Number DYNJ38314G; 62) MINOR SPECIAL PROCEDURE PACK, Pack Number DYNJ38326G; 63) CARDIAC CATH PACK, Pack Number DYNJ38866F; 64) PERM CATH TRAY, Pack Number DYNJ40423AH; 65) O R EMERGENCY PACK, Pack Number DYNJ40460CH; 66) CARDIAC CATH PACK, Pack Number DYNJ40511M; 67) CATH LAB PACK, Pack Number DYNJ40961A; 68) CARDIAC CATH TRAY, Pack Number DYNJ41050C; 69) CATH LAB PACK, Pack Number DYNJ43469D; 70) PK, RADIOLOGY, Pack Number DYNJ43816B; 71) CARDIAC CATH TRAY, Pack Number DYNJ45323F; 72) LEFT HEART, Pack Number DYNJ45984I; 73) CATH LAB PROCEDURE, Pack Number DYNJ46353F; 74) ANGIO PACK, Pack Number DYNJ46401B; 75) CARDIAC CATH TRAY, Pack Number DYNJ46402A; 76) CARDIAC CATH TRAY, Pack Number DYNJ46419C; 77) NEURO CATH PACK (NCLUA)227-LF, Pack Number DYNJ47646D; 78) NEURO CATH PACK (NCLUA)227-LF, Pack Number DYNJ47646F; 79) NEURO CATH PACK (NCLUA)227-LF, Pack Number DYNJ47646G; 80) NEURO

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-2993-2024
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) CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036O; 2) CATH LAB SPECIAL PROCEDURE, Pack Number 00-RDF036OH; 3) CATH ACCESSORY PACK, Pack Number 0M-CP31433J; 4) 3" RADIAL ARTERIAL LINE KIT- OR, Pack Number ART1210; 5) PERF. ASSOC. CUT DOWN TRAY, Pack Number BM17BAD; 6) CATHETER ADD A CATH TRAY, Pack Number CVI4970; 7) BIOPSY TRAY, Pack Number DYNDH1129; 8) ARTHROGRAM TRAY, Pack Number DYNDH1134; 9) BRISTOL MYELOGRAM, Pack Number DYNDH1228; 10) LUMBAR TRAY, Pack Number DYNDH1540A; 11) RADIOLOGY BASIC PACK, Pack Number DYNDH1827; 12) BLOOD CULTURE KIT W/BOTTLES, Pack Number DYNDH1932; 13) BIOPSY PACK, Pack Number DYNDL1462B; 14) CATH LAB PACK-LF, Pack Number DYNJ0105963Q; 15) CARDIAC CATH HARPER PACK-LF, Pack Number DYNJ0161912G; 16) CATH LAB PACK-LF, Pack Number DYNJ0173400P; 17) CATH LAB PACK-LF, Pack Number DYNJ0194968AG; 18) PICC LINE PACK-LF, Pack Number DYNJ0275614F; 19) PEDI CATH PACK-LF, Pack Number DYNJ0429201L; 20) SPECIAL PROCEDURE ANGIO PACK, Pack Number DYNJ04386U; 21) RADIOLOGY PACK, Pack Number DYNJ04562S; 22) IR PACK, Pack Number DYNJ04674U; 23) IR PACK, Pack Number DYNJ04674UH; 24) LEFT HEART PACK-LF, Pack Number DYNJ0490280PH; 25) LT HEART/ANGIOGRAPHY PACK-LF, Pack Number DYNJ0537652AG; 26) SM CARDIAC CATH PACK-LF , Pack Number DYNJ0621195TH; 27) CATH LAB PACK-LF, Pack Number DYNJ0755738R; 28) CARDIAC CATH PACK-LF, Pack Number DYNJ0781476AAH ; 29) CARDIAC CATH PACK-LF, Pack Number DYNJ0781918NH; 30) CATH LAB PACK , Pack Number DYNJ07919GH; 31) PACEMAKER PACK-LF , Pack Number DYNJ0830939ACH ; 32) CARDIAC CATH PACK-LF, Pack Number DYNJ0843627G ; 33) PICC INSERTION PACK-LF, Pack Number DYNJ0880659D; 34) PEDS HEART CATH PACK-LF, Pack Number DYNJ0897998D; 35) RADIAL ARTERY CATH PACK-LF, Pack Number DYNJ0945414BH; 36) RADIAL ARTERY CATH PACK-LF, Pack Number DYNJ0945414CH; 37) CATH LAB PACK , Pack Number DYNJ10117JH; 38) CARDIAC CATH PACK, Pack Number DYNJ17081S; 39) DEPAUL ANGIO PROCEDURE PACK, Pack Number DYNJ19937I; 40) PV/PTA TRAY-RF, Pack Number DYNJ21944VH; 41) ANGIO TRAY, Pack Number DYNJ23438M; 42) ANGIO TRAY, Pack Number DYNJ23438N; 43) ANGIO TRAY, Pack Number DYNJ23438O; 44) ADULT CARDIAC CATH PACK, Pack Number DYNJ23455Q; 45) VIR PACK, Pack Number DYNJ23499MH; 46) HEART CATH-SMH, Pack Number DYNJ24483FH; 47) CATH LAB PACK , Pack Number DYNJ24802PH; 48) ANGIO DRAPE PACK, Pack Number DYNJ24806KH; 49) RADIOLOGY STD TRAY, Pack Number DYNJ25029RH; 50) CARDIAC CATH PACK, Pack Number DYNJ26305N; 51) DIAGNOSTIC ADULT-LF , Pack Number DYNJ27239DH; 52) HEART CATH LT PACK, Pack Number DYNJ31282I; 53) ANGIO PACK, Pack Number DYNJ31339I; 54) CARDIAC CATH PACK, Pack Number DYNJ31847I; 55) NEURO ANGIO TRAY-LF, Pack Number DYNJ34882M; 56) HEART CATH II PACK CHS-LF, Pack Number DYNJ35605M; 57) ISSAQUA CATH/IR PACK, Pack Number DYNJ36738G; 58) PEDS CARDIAC PACK, Pack Number DYNJ37418MH; 59) SPECIAL PROCEDURE PACK-LF, Pack Number DYNJ38050F; 60) SPECIAL PROCEDURE PACK-LF, Pack Number DYNJ38050FH; 61) SPECIAL PROCEDURE PACK, Pack Number DYNJ38314G; 62) MINOR SPECIAL PROCEDURE PACK, Pack Number DYNJ38326G; 63) CARDIAC CATH PACK, Pack Number DYNJ38866F; 64) PERM CATH TRAY, Pack Number DYNJ40423AH; 65) O R EMERGENCY PACK, Pack Number DYNJ40460CH; 66) CARDIAC CATH PACK, Pack Number DYNJ40511M; 67) CATH LAB PACK, Pack Number DYNJ40961A; 68) CARDIAC CATH TRAY, Pack Number DYNJ41050C; 69) CATH LAB PACK, Pack Number DYNJ43469D; 70) PK, RADIOLOGY, Pack Number DYNJ43816B; 71) CARDIAC CATH TRAY, Pack Number DYNJ45323F; 72) LEFT HEART, Pack Number DYNJ45984I; 73) CATH LAB PROCEDURE, Pack Number DYNJ46353F; 74) ANGIO PACK, Pack Number DYNJ46401B; 75) CARDIAC CATH TRAY, Pack Number DYNJ46402A; 76) CARDIAC CATH TRAY, Pack Number DYNJ46419C; 77) NEURO CATH PACK (NCLUA)227-LF, Pack Number DYNJ47646D; 78) NEURO CATH PACK (NCLUA)227-LF, Pack Number DYNJ47646F; 79) NEURO CATH PACK (NCLUA)227-LF, Pack Number DYNJ47646G; 80) NEURO. 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-2993-2024.
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-2993-2024) 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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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).