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FDA Medical Device Recalls (openFDA)

AmeriSource Bergen: MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number for the 50 count box is 57599-7400-4. The NDC number for the 100 count box is 57599-7401-5.

Recall number
Z-0596-04
Recalling firm
AmeriSource Bergen
Product
MediSense Precision QID Blood Glucose Test Strips. The product is sold in box of 50 and 100. The NDC number for the 50 count box is 57599-7400-4. The NDC number for the 100 count box is 57599-7401-5.
Status
Terminated
Initiated
2004-01-30
Posted
2004-07-20
Terminated
2005-05-16
Reason
potential counterfeit product/box
Root cause
Other
Action
The recalling firm issued a recall letter to their direct accounts informing them of the problem and the need to return the product.
Quantity
unknown
Distribution
The products were shipped to retail and hospital pharmacies nationwide, Puerto Rico and the Bahamas.
Lot, serial or model codes
Lot number 89873 exp 4/30/04, Lot number 90524 exp. 11/30/04, Lot number 90848 exp. 1/31/05, Lot number 90891 exp. 1/31/05, and Lot number 91326 exp. 3/31/05.
510(k) numbers
not on file
PMA numbers
not on file
Product code
CGA
Firm FEI
not on file
Firm city
Chesterbrook
Firm state
PA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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