Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

RAPIDFILL Syringe Strip Recalled by Baxter Corporation Englewood Due to Possible breach in sterile barrier for inner and...

Date: April 16, 2014
Company: Baxter Corporation Englewood
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Corporation Englewood directly.

Affected Products

RAPIDFILL Syringe Strip, For use with RAPIDFILL Automated Syringe Filler (ASF): H93890200 RAPIDFILL Syringe Strip, White. H93890221 RAPIDFILL Syringe Strip, Yellow. H93890222 RAPIDFILL Syringe Strip, Orange. H93890223 RAPIDFILL Syringe Strip, Red. H93890225 RAPIDFILL Syringe Strip, Blue. H93890227 RAPIDFILL Syringe Strip, Salmon. H93890229 RAPIDFILL Syringe Strip, Violet. H93890231 RAPIDFILL Syringe Strip, Gray. H93890232 RAPIDFILL Syringe Strip, Green. Sterile 10 ml syringes with twist-off luer sealing tip caps banded together with label material.

Quantity: 774, 600

Why Was This Recalled?

Possible breach in sterile barrier for inner and outer bags of the product.

Where Was This Sold?

This product was distributed to 21 states: AL, AZ, CA, CT, FL, GA, HI, IL, KS, MA, MI, MN, MO, NV, NC, OH, OR, PA, TN, VA, WI

Affected (21 states)Not affected

About Baxter Corporation Englewood

Baxter Corporation Englewood has 9 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report