FDA Recall
OngoingHistorical recordClass II
Array Liquid Antiseptic Handwash, Chloroxylenol 0.1%, NET CONTENTS: 128 FL OZ (1 GAL) 3.785 L, FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE, WYOMING, MI 49509
by Midlab Incorporated
- Reason
- cGMP Deviations: Out of specification results for micro in hand soap products.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
boardwalk ANTIBACTERIAL HANDSOAP REFILL, Chloroxylenol 0.1%, 1 gal. (3.78 L), Manufactured for Essendant Co., One Parkway North, Deerfield, IL 60015
by Midlab Incorporated
- Reason
- cGMP Deviations: Out of specification results for micro in hand soap products.
- Published
- December 11, 2024
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
MAXIM Assure Antibacterial, Chloroxylenol 0.1%, Net Contents: One U.S. Gallon (3.78 L), For Industrial and Institutional Use Only, MIDLAB 140 Private Brand Way, Athens, TN 37303
by Midlab Incorporated
- Reason
- cGMP Deviations: Out of specification results for micro in hand soap products.
- Published
- December 11, 2024
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass I
ZapMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZapMax, 2108 N St. Sacramento, CA 95816, www.zapmax.com
by Boulla LLC
- Reason
- Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
ZoomMax Capsules, 500 mg, 10 count blisters in cartons, Distributed by: ZoomMax, 2108 N St. Sacramento, CA 95816, www.zoommax.com
by Boulla LLC
- Reason
- Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
PeakMax Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: PeakMax, San Francisco, CA, www.PeakMax.com
by Boulla LLC
- Reason
- Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
VitalityXtra Capsules, 500 mg, packaged in 10 count blisters in cartons, Distributed by: VitalityXtra, San Francisco, CA www.vitalityxtra.com
by Boulla LLC
- Reason
- Marketed without an approved NDA/ANDA: Products found to contain undeclared sildenafil and diclofenac.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Venofer (iron sucrose) Injection, USP 100 mg Elemental Iron per 5 mL (20 mg/mL), 5 mL Single-Dose Vials, Rx Only, For Intravenous Use Only, American Regent, Inc. Shirley, NY 11967, NDC: 0517-2340-01 (vial), NDC: 0517-2340-10 (10 x 5 mL/vial cartons), NDC: 0517-2340-25 (25 x 5 mL/vial cartons).
by American Regent, Inc.
- Reason
- Presence of Particulate Matter: Potential for glass delamination from the vials.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Venofer (iron sucrose) Injection, USP 50 mg Elemental Iron per 2.5 mL (20 mg/mL), 2.5 mL Single-Dose Vials, Rx Only, For Intravenous Use Only, Distributed by: Fresenius Medical Care NA, Waltham, MA 02451, NDC: 49230-530-01 (vial), NDC: 49230-530-10 (10 x 2.5mL/vial cartons), NDC: 49230-530-25 (25 x 2.5mL/vial cartons).
by American Regent, Inc.
- Reason
- Presence of Particulate Matter: Potential for glass delamination from the vials.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Venofer (iron sucrose) Injection, USP 100 mg Elemental Iron per 5 mL (20 mg/mL), 5 mL Single-Dose Vials, Rx Only, For Intravenous Use Only, Distributed by: Fresenius Medical Care NA, Waltham, MA 02451, NDC: 49230-534-01 (vial), NDC: 49230-534-25 (25 x 5 mL/vial cartons).
by American Regent, Inc.
- Reason
- Presence of Particulate Matter: Potential for glass delamination from the vials.
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Cinacalcet Tablets, 90 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-833-30), b) 500-count HDPE bottle (NDC 65862-833-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India. 90 mg - 30 Tablets - NDC 65862-833-30 90 mg - 500 Tablets - NDC 65862-833-05
by Aurobindo Pharma USA Inc
- Reason
- cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Cinacalcet Tablets, 60mg, packaged in: a) 30-count HDPE bottle (NDC 65862-832-30), b) 500-count HDPE bottle (NDC 65862-832-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India.
by Aurobindo Pharma USA Inc
- Reason
- cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
- Published
- December 11, 2024
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Cinacalcet Tablets, 30 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-831-30); b) 500-count HDPE bottle (NDC 65862-831-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India.
by Aurobindo Pharma USA Inc
- Reason
- cGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
- Published
- December 11, 2024
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-449-17
by ACCORD HEALTHCARE, INC.
- Reason
- Subpotent drug
- Published
- December 11, 2024
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: December 31, 2024Historical recordClass I
Albertsons Companies LLC
- Product
- (1) GINGER CHICKEN BROCCOLI SALAD FS (UPC 27110800000) (2) R…
- Reason
- Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
- Published
- December 11, 2024
- Distribution
- AK, AZ, AR, CA, ID, IL, IN, IA, LA, ME,…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: December 31, 2024Historical recordClass II
Albertsons Companies LLC
- Product
- (1) READY MEALS CHICKEN STREET TACOS SS COLD (UPC 2713160000…
- Reason
- Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
- Published
- December 11, 2024
- Distribution
- AK, AZ, AR, CA, ID, IL, IN, IA, LA, ME,…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: December 31, 2024Historical recordClass II
Albertsons Companies LLC
- Product
- (1) READY MEALS GREEN CHILI CHICKEN ENCHILADAS SS COLD (UPC…
- Reason
- Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
- Published
- December 11, 2024
- Distribution
- AK, AZ, AR, CA, ID, IL, IN, IA, LA, ME,…
View recall →
FDA Recall
🇺🇸 United States
CompletedHistorical recordClass II
DYMA BRANDS
- Product
- MONARCH INSTANT CHOCOLATE PUDDING & PIE FILLING MIX NATURALL…
- Reason
- After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
- Published
- December 11, 2024
- Distribution
- Products were distributed to the followi…
View recall →
FDA Recall
🇺🇸 United States
CompletedHistorical recordClass II
DYMA BRANDS
- Product
- THIRSTER LOW CAL FRUIT, NET WT. 8.6OZ, Case UPC 507581083973…
- Reason
- After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
- Published
- December 11, 2024
- Distribution
- Products were distributed to the followi…
View recall →
FDA Recall
🇺🇸 United States
CompletedHistorical recordClass II
DYMA BRANDS
- Product
- THIRSTER Lemonade Drink Mix NATURALLY FLAVORED LOW CALORIE,…
- Reason
- After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
- Published
- December 11, 2024
- Distribution
- Products were distributed to the followi…
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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