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RecallWatchMedical Device Safety
Device type

Labor And Delivery Kit recalls

The FDA has posted 9 enforcement recalls of labor and delivery kit devices since 2025, including 1 Class I (most serious) recall. Most recent report: Sep 9, 2026.

Class I: 1Class II: 8

Who is recalling these devices

Class IIOngoingZ-3059-2026

Medline Industries, LP recalls Medline Convenience Kits: 1) LABOR CDS

The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area.…

  • Labor And Delivery Kit
  • Nonconforming Material/Component
Medline Industries, LPILSep 9, 2026
Class IIOngoingZ-2108-2026

Medline Industries, LP recalls Medline Convenience Kits: 1) OB KIT

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles;…

  • Labor And Delivery Kit
  • Process control
Medline Industries, LPILMay 13, 2026
Class IOngoingZ-1727-2026

Medline Industries, LP recalls Medline medical convenience kits

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the s…

  • Labor And Delivery Kit
  • Under Investigation by firm
Medline Industries, LPILApr 15, 2026
Class IIOngoingZ-1414-2026

Medline Industries, LP recalls Medline Convenience Kits: 1) OB KIT

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles;…

  • Labor And Delivery Kit
  • Under Investigation by firm
Medline Industries, LPILFeb 25, 2026

Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Labor And Delivery Kit”). Informational only — verify against the FDA before acting.