11.20.2003

IMMEDIATE ACTION REQUIRED!! The FDA has announced a recall of all drug products containing PPA (phenylpropanolamine). The AAFES stock assortment contains 23 products containing this drug (see below) .... ALL MUST BE PULLED FROM SALE IMMEDIATELY and placed in controlled storage pending disposition instructions. In addition, customers presenting unused quantities of these items purchased from AAFES may be given full refunds. Locally printed signs will be placed as follows:

CRC Description
----------------------------
5252333 ALKA-SELTZER PLUS
1350966 TAVIST-D
7388036 TRIAMINIC TRIAMINICOL
9175688 CONTACT SEVERE COLD 16 CT
1190814 COMTREX DEEP CHEST 24 CT
7533225 DEXATRIM XS W/VIT C
6400584 DEXATRIM EXT DURATION (PHASE-OUT STATUS)
3131711 ACCUTRIM MAXIMUM STRENGTH
1307750 DIMETAPP DM COUGH/COLD
3028438 DIMETAPP ELIXER
1216522 ALKA SELTZER PLUS COLD LIQUID
3709664 ALKA SELTZER PLUS NIGHT TIME (PHASE OUT STATUS)
5275920 ALKA SELTZER PLUS ORANGE
3782000 ALKA SELTZER PLUS TABS
3509700 ALKA SELTZER PLUS NIGHT TIME TABS
7730608 AAFES TUSSIN CF COUGH FORMULA 4 OZ.
8515727 AAFES DIMAPHEN ELIXIR 4 OZ.
8093916 AAFES EFFERVESCENT COLD RELIEF 36 COUNT
3024833 AAFES DIET CAPLETS
8147803 PERMATHENE-16
3247319 ROBITUSSIN CF COUGH SYRUP
3114808 COMTREX MULTI SYMPTOM
3377900 SINE OFF SINUS

This recall action is mandatory and should be accomplished as soon as possible. Report compliance to respective Region retail offices via TAO. Contact CARTERRE with questions.

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