medical MODERATE Updated 2022-10-05

CooperSurgical, Inc. recalls Humidifier bottle and syringe filter kit (6 count of each) f

See all recalls from CooperSurgical, Inc. →

Recalled Product

Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark II Benchtop Incubator (AY200246)

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

There is a potential breach to the sterile barrier containing the Humidifier Bottles due to the packaging of the filter box located inside the bottle packaging. Damage to the sterile barrier may result in use of an unsterilized device, which may cause contamination and degradation or loss of embryo during incubation.

Issued by

FDA

Affected States: AL, AZ, CA, CT, DE, FL, GA, HI, IL, KS, MA, MI, MN, MO, NJ, NY, OH, OR, SC, TX, VA, VT, WA, WI, WV
Lot/Code Info: Lot Numbers 18-1265 18-1268 18-1268 / G004639 G004637 G004638 G004639

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Humidifier bottle and syringe →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

Medline Industries, LP recalls Medline Convenience Kits: 1) MAJOR PACK, Catalog Number: DY

2026-09-30 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

Medline Industries, LP recalls Medline Convenience Kits: 1) PEDS SINUS PACK, Catalog Numbe

2026-09-30 · The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

Philips North America Llc recalls SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T

2026-09-30 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.

Philips North America Llc recalls Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T Initi

2026-09-30 · A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the available system memory.