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FDA Medical Device Recalls (openFDA)

Pointe Scientific, Inc.: Calcium Reagent Set. Pointe Scientific Liquid Hitachi Calcium Reagent Set, Pointe Scientific, Inc, Canton, MI; Catalog #'s HC902-576 and HC902-1000. Calcium Reagent Set for repackaging, Catalog # HC902-SAM-911. The product is used for the quantitative determination of calcium in serum on Hitachi analyzers.

Recall number
Z-1041-2010
Recalling firm
Pointe Scientific, Inc.
Product
Calcium Reagent Set. Pointe Scientific Liquid Hitachi Calcium Reagent Set, Pointe Scientific, Inc, Canton, MI; Catalog #'s HC902-576 and HC902-1000. Calcium Reagent Set for repackaging, Catalog # HC902-SAM-911. The product is used for the quantitative determination of calcium in serum on Hitachi analyzers.
Status
Terminated
Initiated
2009-11-10
Posted
2010-03-10
Terminated
2010-12-10
Reason
Non-compliance with the Good Manufacturing Practice regulations, as the manufacturing process for this product had not been validated.
Root cause
Process control
Action
Consignees were notified by "Urgent: Medical Device Recall" letter dated November 11, 2009 and instructed to conduct a recall to the retail level, that users should dispose of the product immediately, and that a business reply card should be returned to account for products. If you have any questions, please call Pointe Scientific, Inc. Technical Support Department at 1-800-757-5313 or 1-734-487-8300.
Quantity
44 sets
Distribution
Worldwide Distribution (United States, Chile, India, Republic of Yemen and Trinidad).
Lot, serial or model codes
All lots containing 813401 as part of the lot number.
510(k) numbers
["K822469"]
PMA numbers
not on file
Product code
CIC
Firm FEI
1827821
Firm city
Canton
Firm state
MI
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

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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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