Mucolytic Agent 1 pint/473 ml recall: Contamination
Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology…
Why was Mucolytic Agent 1 pint/473 ml recalled?
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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Richard Allan Scientific Mucolytic Agent 1 pint / 473 ml Product code: 76166, Lot #s and EXP Dates: 313839-Dec 2016; 311157-Oct-2016; 306726-Aug-2016; 297142-Jun-2016; 296289-May-2016; 290486-Mar-2016; 289488-Mar-2016; 276824-Nov-2015; 271110-Oct-2015; 265368-Aug-2015. Richard Allan Scientific Mucolytic Agent 1 gallon/ 3.8 l, Product Code: 76167; Lot Number & EXP Dates: 311158- Oct-2016; 302099- Jun-2016; 298834-Jun-2016; 293734- Apr-2016; 288009-Feb-2016; 283396-Jan-2016; 279581-Nov-2015; and 274814- Oct-2015 Dec-2016 Oct-2016 Aug-2016 Jun-2016 May-2016 Mar-2016 Mar-2016 Nov-2015 Oct-2015 Aug-2015
- Product
- Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology…
- Recalling firm
- Richard-Allan Scientific Company
- Quantity
- Product 76166- 116; Product Code 76167-29
- Distribution
- Worldwide Distribution - US Nationwide in the states of: AR; AZ; CA; CO; FL; GA; I A; IL; IN; KY; MA; MN; MO; MS; MT; NC; ND; NJ; NV; NY; OH; OK; PA; PR; SD; TN; TX; VA; WA; WI and the countries of: Bangladesh, Canada, China, Costa Rica, Dubai, France, Germany, Greece, India, Ireland, Israel, Italy, Japan, Korea, Netherlands, Panama, Poland, Portugal, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, and UK.
- Recall date
- May 27, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)