Reported Mar 6, 2013 · Terminated
Bronkaid Dual Action Formula, Ephedrine Sulfate 25 mg/Bronchodilator, Guaifenesin 400 mg/Expectorant, a) 24 coated…
Bayer Healthcare, LLC
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Bayer Healthcare, LLC · 36 Columbia Rd · Morristown, NJ · 07960-4526
Is this the product you have?
Bronkaid Dual Action FormulaEphedrine Sulfate 25 mg/BronchodilatorGuaifenesin 400 mg/Expectoranta) 24 coated caplets per blister packUPC 300240537879b) 60 coated caplets per blister packUPC 300240537855Bayer HealthCare LLCConsumer CareP.O. Box 1910MorristownNJ07962
- Lot codes and dates
Lot #s: a) NAA0B3TNAA0BDBNAA0B3PNAA0B3RNAA0B3NNAA070ENAA070FNAA03PXNAA03B5NAA03B6NAA02LT. b) NAA0TF3NAA0TF2NAA0TF0NAA0TF1NAA0TETNAA0TEWNAA0TEXNAA0HHLNAA0HHKNAA0HHNNAA0HHHNAA0DK5NAA0DK4NAA0DK3NAA0CHENAA0CHDNAA0B3LNAA0B3KNAA09XENAA09XBNAA07H2NAA09XDNAA07H1NAA09XANAA09XCNAA07H3NAA07H4NAA05BBNAA05BANAA07H0NAA070DNAA070CNAA03PWNAA05B9NAA070BNAA03B8NAA03B7NAA02N1NAA02LW244511P244501P244481P244471P244491P244451P
- Amount recalled
- 1,353,420 Blister Packs
Where it was sold
- Nationwide
Why it was recalled
Labeling: Label lacks warning or Rx legend; Certain information was inadvertently excluded from the product carton label.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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