Greiner Bio-One North America, Inc. 2022-01-26 Health serious FDA
Health · FDA · Recall #FDA-Z-0502-2022
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring,… Recall
Issued January 26, 2022 · Greiner Bio-One North America, Inc.
In January 2022, Greiner Bio-One North America, Inc. recalled the greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Some of the blood collection tubes show clotting due to variation of Lithium Heparin.
What you should do
- 1 Stop using greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Greiner Bio-One North America, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Greiner Bio-One North America, Inc.
- Category
- Health
- Recall date
- January 26, 2022
- Units affected
- Not reported
- Sold at
- Distribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA. There was no foreign/military/government distribution.
- Recall number
- FDA-Z-0502-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Greiner Bio-One North America, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.