Data Foundry

Medical device recalls 2017

Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid… — Class II medical device recall Z-1895-2017

Terminated recall by Richard-Allan Scientific Company, reported 2017-05-10, distributed in CA, CO, CT, DE, GA, HI, IA, IL…. Methylene Blue, Solution #3 in the Kwik Diff Kit was not Methylene Blue but Crystal Violet instead.

Recall numberZ-1895-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmRichard-Allan Scientific Company, Kalamazoo, MI, United States
Recall initiated2017-03-15
Classified2017-04-28
Reported by FDA2017-05-10
Terminated2017-07-27
DistributedCA, CO, CT, DE, GA, HI, IA, IL, KS, MA, MS, NC, NH, NM, NY, OH, PA, PR, RI, UT, VA, VT, WA, WV
Quantity390
Lot numbers234, 235, 236, S-645, S-646, S-647
Model numbers9990700, 9990707
Expiration dates2018-08-18

Product

Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707 Shandon Rapid Chrome Kwik-Diff Kit, Part Number 9990700 is sold as a kit in 500ml bottles. Shandon Rapid Chrome Kwik-Diff Kit, Part Number 9990707 is sold as a reagent in a 4L bottle. Intended for use as a kit in special stain techniques.

Reason for recall

Methylene Blue, Solution #3 in the Kwik Diff Kit was not Methylene Blue but Crystal Violet instead.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1895-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.