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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 65111

6 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 07, 2013
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Novartis Consumer Health

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

6 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 6

Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings) bottles, UPC 300670068356, 9.4-oz (58 servings) bottles, UPC 300670068585, and 18.7-oz. (115 servings) bottles, UPC 300670068158. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, Made in France.

F-1959-2013
Recall number
F-1959-2013
Initiated
May 07, 2013
Classification
Class II
Status
Terminated
Recalling firm
Novartis Consumer Health
Quantity
226,381 consumer units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products are being recalled due to the receipt of a relatively high number of consumer complaints.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Code information

5.7-oz. (35 servings) bottles: 10100230; 9.4-oz. (58 servings) bottles: 10119358, 10121489, 10121490, 24596401, 24596402, 24680101, and 24767601; and 18.7-oz. (115 servings) bottles: 24596701.

Distribution pattern

Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.

food · product 2 of 6

Benefiber Plus Heart Health Non-Thickening Powder, Sugar Free, packaged in 6.4-oz (48 servings) bottles, UPC 300673002487. Distributed by: Novartis Consumer health, Inc., Parsippany, NJ 07054-0622. Made in France.

F-1960-2013
Recall number
F-1960-2013
Initiated
May 07, 2013
Classification
Class II
Status
Terminated
Recalling firm
Novartis Consumer Health
Quantity
170,220/6.4-oz. (48 servings) bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products are being recalled due to the receipt of a relatively high number of consumer complaints.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Code information

10118915, 10118916, 10118917, 10118918, 10120338, 10120361, 10122590, 10122591, 10123950, 10126662, and 10127376

Distribution pattern

Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.

food · product 3 of 6

Benefiber Fiber Drink Mix, Cherry Pomegranate, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670107246. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

F-1961-2013
Recall number
F-1961-2013
Initiated
May 07, 2013
Classification
Class II
Status
Terminated
Recalling firm
Novartis Consumer Health
Quantity
162,408/5.0-oz. (24-ct) boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products are being recalled due to the receipt of a relatively high number of consumer complaints.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Code information

10116609, 10118436, 10121279, 10121280, 10122653, 10122654, 10125466, and 10128711

Distribution pattern

Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.

food · product 4 of 6

Benefiber Fiber Drink Mix, Kiwi Strawberry, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670106249. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

F-1962-2013
Recall number
F-1962-2013
Initiated
May 07, 2013
Classification
Class II
Status
Terminated
Recalling firm
Novartis Consumer Health
Quantity
152,016/5.0-oz. (24-ct) boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products are being recalled due to the receipt of a relatively high number of consumer complaints.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Code information

10114419, 10115003, 10118673, 10121091, 10121092, 10121093, 10121094, 10123826, 10125460, and 10125461

Distribution pattern

Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.

food · product 5 of 6

Benefiber Fiber Supplement Plus Calcium, Orange Natural Flavor, Sugar Free, packaged in 10.76-oz (48 Servings) bottles, UPC 300670108489. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

F-1963-2013
Recall number
F-1963-2013
Initiated
May 07, 2013
Classification
Class II
Status
Terminated
Recalling firm
Novartis Consumer Health
Quantity
110,664/10.76-oz (48 Servings) bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products are being recalled due to the receipt of a relatively high number of consumer complaints.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Code information

10102129, 10102130, 10102131, 10104656, 10104657, 10104658, 10104659, 10107484, 10114954, 10124211, and 10125514

Distribution pattern

Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.

food · product 6 of 6

Benefiber Non-Thickening Powder, Sugar Free, packaged in the following configurations: (1) 2.8-oz. (20 servings) bottles, UPC 300670044206; (2) 4.6-oz. (32 servings) bottles, UPC 300670044329; (3) 5.4-oz. (38 servings) bottles, UPC 300670044381; (4) 8.6-oz. (62 servings) bottles, UPC 300670044626; (5) 12.3-oz. (90 servings) bottles, UPC 300670044909; (6) 16.7-oz. (125 servings) bottles, UPC 300670044831; (7) 1.6-lb. (190 servings) bottles, UPC 300670044190; (8) 20.2-oz .(125+25=150 servings) bottles, UPC 300670174590; (9) 10.3-oz. (62+13=75 servings) bottles, UPC 300670175757; (10) Bulk .12-oz. (1 serving) stick pack, UPC 300679999996; (11) 3.45-oz. boxes containing 28/0.12-oz. stick packs, UPC 300670030285; and (12) 4.19-oz. boxes containing 28+6/0.12-oz. stick packs, UPC 300670030346. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

F-1964-2013
Recall number
F-1964-2013
Initiated
May 07, 2013
Classification
Class II
Status
Terminated
Recalling firm
Novartis Consumer Health
Quantity
19,900,520 consumer units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The products are being recalled due to the receipt of a relatively high number of consumer complaints.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Code information

2.8-oz. (20 servings) bottles: 10081233, 10084981, 10086954, 10087654, 10089097, 10090985, 10095687, 10095688, 10102413, 10102758, 10106405, 10107215, 10110117, 0112155, 10115504, 10119610, 10120346, 10123373, and 10124210; 4.6-oz. (32 servings) bottles: 10093120, 10099454, 10101273, 10102759, 10104643, 10107322, 10107334, 10109690, 10114152, and 10123951; 5.4-oz. (38 servings) bottles: 10079944, 10079945, 10084982, 10086957, 10087655, 10088811, 10089098, 10089099, 10090986, 10090987, 10095505, 10097339, 10101278, 10102700, 10104644, 10104645, 10104646, 10104647, 10107225, 10108800, 10112148, 10112149, 10116295, 10117967, 10118825, 10120029, 10120452, and 10122150; 8.6-oz. (62 servings) bottles: 10081004, 10081005, 10081006, 10081007, 10081008, 10081009, 10081010, 10081011, 10087657, 10087658, 10089129, 10089130, 10089131, 10090593, 10090992, 10090993, 10090998, 10090999, 10093121, 10094588, 10095506, 10099453, 10101280, 10102760, 10104648, 10104649, 10107227, 10107232, 10108547, 10108549, 10108550, 10112145, 10116296, 10117966, 10118824, 10120023, 10120341, 10120449, 10122151, and 10122152; 12.3-oz. (90 servings) bottles: 10081000, 10081001, 10081002, 10081003, 10084983, 10086955, 10086956, 10087662, 10087663, 10089133, 10089134, 10095507, 10097341, 10101281, 10109497, 10112175, 10115077, 10119609, 10120348, and 10122866; 16.7-oz. (125 servings) bottles: 10080810, 10081012, 10081013, 10081114, 10086958, 10087661, 10089135, 10089136, 10090988, 10090989, 10093124, 10095503, 10095510, 10102761, 10104650, 10104652, 10104654, 10107344, 10112146, 10112147, 10116297, 10117964, 10118823, 10120008, 10120345, 10120799, 10121700, 10122154, 10122956, and 10127499; 25.6-oz. (190 servings) bottles: 10081227, 10081228, 10081229, 10081230, 10081231, 10081232, 10084984, 10084985, 10084986, 10084987, 10084988, 10087659, 10087660, 10089137, 10089138, 10090994, 10090995, 10090996, 10095513, 10095514, 10102762, 10102763, 10104655, 10107381, 10108545, 10112153, 10113299, 10118822, 10120006, 10122129, 10122230, 10122458, and 10124273; 20.2-oz. (125+25=150 servings) bottles: 10100270, 10100272, and 10120315; 10.3-oz. (62+13=75 servings) bottles: 10106742, 10109551, 10111859, 10116666, and 10123229; Bulk .12-oz. (1-ct.) stick packs: 24621901, 24621902, 24621903, 24621904, 24807701, 24807702, 24807703, 24807704, 24807705, 24807706, 24807707, 24930501, 24930502, 24930503, 24930504, 25318601, 25318602, 25318603, and 25318604; 3.45-oz. (28-ct. stick pack) boxes: 10115152, 10115284, 10115617, 10116201, 10116301, 10116302, 10116604, 10121341, 10122650, 10127826, 10113682A, 10114422A, 24329201, 24329202, 24329203, 24329204, 24506601, 24506602, 24596603, 24596604, 24596605, 24767501, 24767502, 24767503, 24767504, 24767506, 24767507, 25239401, 25239402, 25239403, 25239404, 25239405, 25239406, 25239407, 25239408, 25239409, and 25239410; and 4.19-oz. (28+6 stick pack) boxes: 10107198, 10116607, 10116608, 10122652, and 10122934.

Distribution pattern

Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.