Hardy Diagnostics recalls Quickslide GramPro 1 microscope slide stainers with specific lot and serial numbers due to defective tubing in the pump mechanism.
Instruments were assembled and serviced using a defective lot of tubing, which is part of the pump mechanism within the unit.
Hardy Diagnostics is recalling specific models of their Quickslide GramPro 1 microscope slide stainers because they were assembled with defective tubing that could cause malfunction. This recall affects users who own the recalled units and may impact laboratory or educational settings where these devices are used.
The stainers were assembled using a defective lot of tubing that is part of the pump mechanism. This defect could lead to improper functioning of the device, potentially causing inaccurate staining results or other operational issues.
Users of the Quickslide GramPro 1 microscope slide stainers with the listed lot and serial numbers are affected. Laboratory professionals and educational institutions using these devices are most at risk.
Check the lot numbers (1654, 1657, 1658, 1660, 1661, 1662, 1663) and serial numbers (354, 417, 422, 462, 472, 473, 480, 488, 490, 491, 496, 503, 505, 513, 521, 522, 526, 536, 551, 562, 564, 589, 590, 592, 596, 603, 606, 616, 620, 621, 622, 623, 624, 625, 626, 627, 628, 629, 630, 631, 632, 633, 634, 635, 636, 637, 638, 639, 640, 641, 642, 643, 644, 645, 646, 647, 648, 649, 650, 651, 652, 653, 654, 655, 656, 657, 658, 2005, 2012) to determine if your unit is recalled.
Identify your unit's lot numbers (1654, 1657, 1658, 1660, 1661, 1662, 1663) and serial numbers (354, 417, 422, 462, 472, 473, 480, 488, 490, 491, 496, 503, 505, 513, 521, 522, 526, 536, 551, 562, 564, 589, 590, 592, 596, 603, 606, 616, 620, 621, 622, 623, 624, 625, 626, 627, 628, 629, 630, 631, 632, 633, 634, 635, 636, 637, 638, 639, 640, 641, 642, 643, 644, 645, 646, 647, 648, 649, 650, 651, 652, 653, 654, 655, 656, 657, 658, 2005, 2012) to see if it's recalled.
The Quickslide GramPro 1 is a microscope slide stainer used for laboratory or educational purposes.
Check the lot numbers (1654, 1657, 1658, 1660, 1661, 1662, 1663) and serial numbers (354, 417, 422, 462, 472, 473, 480, 488, 490, 491, 496, 503, 505, 513, 521, 522, 526, 536, 551, 562, 564, 589, 590, 592, 596, 603, 606, 616, 620, 621, 622, 623, 624, 625, 626, 627, 628, 629, 630, 631, 632, 633, 634, 635, 636, 637, 638, 639, 640, 641, 642, 643, 644, 645, 646, 647, 648, 649, 650, 651, 652, 653, 654, 655, 656, 657, 658, 2005, 2012) listed in the recall notice.
The recall notice does not specify a remedy, so no action is required beyond checking if your unit is in the recalled list.
We’ve drafted a message you can send Hardy Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1835-2021 — Hardy Diagnostics Hardy Diagnostics Hello, I own a Hardy Diagnostics that is covered by recall Z-1835-2021 from Hardy Diagnostics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
