greiner bio-one VACUETTE TUBE recall
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF…
Why was greiner bio-one VACUETTE TUBE recalled?
Some of the blood collection tubes show clotting due to variation of Lithium Heparin.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #B21053QG, Exp. 09/09/2022, UDI: Case: 39120017579046, Rack: 29120017579049.
- Product
- greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF…
- Recalling firm
- Greiner Bio-One North America, Inc.
- Quantity
- 889,200 pcs.
- Distribution
- Distribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA. There was no foreign/military/government distribution.
- Recall date
- January 26, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)