Reckitt Benckiser LLC: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: September 2, 2015. Most recent: March 20, 2019.

Risk classification: Class I: 2 · Class II: 2 · Class III: 1

Most recent recalls

DateAgencyProduct
March 20, 2019FDADurex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00 02340…Z-0994-2019
March 1, 2017FDADurex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated la…Z-1249-2017
September 28, 2016FDAMucinex Sinus-Max Day Night, 60 caplets, Dist. by Reckitt Benckiser, Parsippany, NJ 07054…D-1517-2016
September 2, 2015FDAMucinex Fast Max Night Time Cold & Flu, Maximum Strength, Acetaminophen Pain Reliever/Fev…D-1364-2015
September 2, 2015FDAMucinex Fast Max Cold, Flu & Sore Throat, Maximum Strength, Acetaminophen Pain Reliever/F…D-1363-2015

Questions about this company

How many recalls does Reckitt Benckiser LLC have?
Recalert has 5 U.S. recalls on record for Reckitt Benckiser LLC, published between September 2, 2015 and March 20, 2019.
What was the most recent Reckitt Benckiser LLC recall?
FDA recall Z-0994-2019, published March 20, 2019: Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00
Which agencies have handled Reckitt Benckiser LLC recalls?
Reckitt Benckiser LLC appears as the recalling firm in recalls from: FDA (5).

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