medical MODERATE Updated 2025-02-26

Remel, Inc recalls remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for

See all recalls from Remel, Inc →

Recalled Product

remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI 848838003684, Lot Number 213971, exp. 2025-02-25

✅ 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 remel BLOOD AGAR EMB →

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

Baxter Healthcare Corporation recalls Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Cir

2026-07-08 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

Medline Industries, LP recalls Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY,

2026-07-08 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Medline Industries, LP recalls Medline Convenience Kits: 1) MULTIMED, 7FR, 20CM, 3L, CVC B

2026-07-08 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circ

2026-07-08 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.