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Richard-Allan Scientific LLC

United States·US-MF-000008261

Last updated September 17, 2026

Information

Country: United States
Address: 4481 Campus Drive, Kalamazoo, United States
Website: epredia.com
LinkedIn: —
Facebook: —
Email: #[email protected]
Phone: —
PRRC Contact: Naveen Kaki
EUDAMED SRN: US-MF-000008261
FDA FEI Number: 1831638
DUNS Number: —

Catalogue (1838)

Page 1 of 37

Device	Model / Reference	Registries	Class	Status
Thermo Scientific	TL-125-ALJ	FDA UDI	Class I	Active
Thermo Scientific	MS-1498-R7	FDA UDI	Class I	Active
Thermo Scientific	MS-321-R7	FDA UDI	Class I	Active
Epredia	Microtome Knife C-Profile 240 mm	FDA UDI	Class I	Active
Thermo Scientific	RM-9106-RQ	FDA UDI	Class I	Active
Thermo Scientific	RB-9010-R7	FDA UDI	Class I	Active
Thermo Scientific	TL-125-HLJ	FDA UDI	Class I	Active
Thermo Scientific	MS-376-S0	FDA UDI	Class I	Active
Thermo Scientific	TA-999-QHDX	FDA UDI	Class I	Active
Thermo Scientific	MS-363-P0	FDA UDI	Class I	Active
Thermo Scientific	MS-1603-P	FDA UDI	Class I	Active
Thermo Scientific	RB-9291-R7	FDA UDI	Class I	Active
Thermo Scientific	MS-409-P	FDA UDI	Class I	Active
Thermo Scientific	MS-799-P1	FDA UDI	Class I	Active
Thermo Scientific	MS-457-R7	FDA UDI	Class I	Active
Thermo Scientific	MS-1237-P	FDA UDI	Class I	Active
Thermo Scientific	MS-397-R7	FDA UDI	Class I	Active
Thermo Scientific	RB-9035-P0	FDA UDI	Class I	Active
Thermo Scientific	MS-180-P	FDA UDI	Class I	Active
Thermo Scientific	MS-1352-P1	FDA UDI	Class I	Active
Thermo Scientific	MS-1932-P0	FDA UDI	Class I	Active
Thermo Scientific	MS-1947-R7	FDA UDI	Class I	Active
Thermo Scientific	MS-341-P1	FDA UDI	Class I	Active
Thermo Scientific	RM-2103-S0	FDA UDI	Class I	Active
Thermo Scientific	MS-1856-RQ	FDA UDI	Class I	Active
Thermo Scientific	TA-060-AF	FDA UDI	Class I	Active
Thermo Scientific	MS-321-P0	FDA UDI	Class I	Active
Thermo Scientific	TL-060-HLJ	FDA UDI	Class I	Active
Thermo Scientific	MS-10637-P	FDA UDI	Class I	Active
Thermo Scientific	MS-1857-P	FDA UDI	Class I	Active
Thermo Scientific	RM-2100-R7	FDA UDI	Class I	Active
Thermo Scientific	RB-9038-R7	FDA UDI	Class I	Active
Thermo Scientific	RB-9002-P0	FDA UDI	Class I	Active
Thermo Scientific	MS-1941-S	FDA UDI	Class I	Active
Epredia	RM-2104-RQ-A	FDA UDI	Class I	Active
Thermo Scientific	MS-1157-S0	FDA UDI	Class I	Active
Thermo Scientific	RM-9121-S	FDA UDI	Class I	Active
Thermo Scientific	MS-180-P0	FDA UDI	Class I	Active
Thermo Scientific	MS-397-RQ	FDA UDI	Class I	Active
Thermo Scientific	MS-1149-P1	FDA UDI	Class I	Active
Thermo Scientific	RM-2102-R7	FDA UDI	Class I	Active
Thermo Scientific	MS-129-P0	FDA UDI	Class I	Active
Thermo Scientific	MS-1458-S1	FDA UDI	Class I	Active
Thermo Scientific	RM-9132-S	FDA UDI	Class I	Active
Thermo Scientific	RB-1433-R7	FDA UDI	Class I	Active
Thermo Scientific	RB-1433-A1	FDA UDI	Class I	Active
Thermo Scientific	RM-2124-RQ	FDA UDI	Class I	Active
Thermo Scientific	MS-1498-S	FDA UDI	Class I	Active
Thermo Scientific	RB-281-R7	FDA UDI	Class I	Active
Epredia	Sodium Bicarbonate Solution	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

Epredia Netherlands B.V. NL

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (15)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jun 4, 2018	Z-2749-2018	—	terminated	Mislabeled product
Mar 15, 2017	Z-1895-2017	—	terminated	Methylene Blue, Solution #3 in the Kwik Diff Kit was not Methylene Blue but Crystal Violet instead.
Jun 13, 2016	Z-2351-2016	—	terminated	potential contamination with potassium hydroxide may have an impact when performing immunohistochemistry testing. It is unknown whether the contamination will affect tissue antigenicity. If it were to affect tissue antigenicity, the outcome would be risk of false positive or false negative test results which may lead to serious injury. There is the possibility the patient may need to be re-biopsied.
Feb 16, 2016	Z-1319-2016	—	terminated	Multiple complaints were received from customers indicating that they ordered product 8335(Type 3 Paraffin) but when they opened the box, they found product 8336 (Type 6 Paraffin) inside.
Apr 29, 2015	Z-1639-2015	—	terminated	Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and Mucolexx following a customer complaint reporting that a lab had found fungal contamination in 2 lots of Mucolexx.
Apr 29, 2015	Z-1640-2015	—	terminated	Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and Mucolexx following a customer complaint reporting that a lab had found fungal contamination in 2 lots of Mucolexx.
Feb 19, 2015	Z-1264-2015	—	terminated	The case was correctly labeled as REF 7501R, however the gallon bottle was incorrectly labeled as REF 7501G Cyto-Stain G. The bottle label has the correct lot number of 313833 and EXP date 11/2016. The gallon bottle contains the correct intended contents of 7501R: Cyto-Stain R Stain.
Sep 17, 2014	Z-0012-2015	—	terminated	The affected lots could have NBF concentrations that are lower or higher than the desired specifications.
Sep 17, 2014	Z-0018-2015	—	terminated	The affected lots could have NBF concentrations that are lower or higher than the desired specifications.
Sep 17, 2014	Z-0017-2015	—	terminated	The affected lots could have NBF concentrations that are lower or higher than the desired specifications.
Sep 17, 2014	Z-0015-2015	—	terminated	The affected lots could have NBF concentrations that are lower or higher than the desired specifications.
Sep 17, 2014	Z-0013-2015	—	terminated	The affected lots could have NBF concentrations that are lower or higher than the desired specifications.
Sep 17, 2014	Z-0014-2015	—	terminated	The affected lots could have NBF concentrations that are lower or higher than the desired specifications.
Sep 17, 2014	Z-0016-2015	—	terminated	The affected lots could have NBF concentrations that are lower or higher than the desired specifications.
Aug 12, 2011	Z-0039-2012	—	terminated	The firm has received two complaints of finger lacerations in operators of this device.