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Recalls affecting Mississippi

Data last updated: September 8, 2026 at 1:13 PM UTC

16,726 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
Class IHigh risk
FoodBacteria/virusRecalled July 17, 2026

Cross Valley Farms LETTUCE CHOP 4/5# Cross Valley Farms LETTUCE SHRED 1/4" 4/5# Cross Valley Farms LETTUCE SHRED 1/8" 4/5# Iceberg only products.

Potential Cyclospora contamination.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1279-2026
Lot/product code:
Cross Valley Farms LETTUCE CHOP 4/5# TFMX183A04 7/20/2026 TFMX184A03 7/21/2026 TFMX188A02 7/25/2026 TFMX190A02 7/27/2026 TFMX195B04 8/1/2026 Cross Valley Farms LETTUCE SHRED 1/4" 4/5# TFMX182A04 7/19/2026 TFMX183A01 7/20/2026 TFMX184B01 7/21/2026 TFMX185A04 7/22/2026 TFMX187B03 7/24/2026 TFMX188A04 7/25/2026 TFMX190A04 7/27/2026 TFMX190B01 7/27/2026 TFMX191A04 7/28/2026 TFMX194B03 7/31/2026 TFMX196A02 8/2/2026 Cross Valley Farms LETTUCE SHRED 1/8" 4/5# TFMX183A04 7/20/2026 TFMX184A04 7/21/2026 TFMX185A01 7/22/2026 TFMX187B03 7/24/2026 TFMX188A04 7/25/2026 TFMX189A03 7/26/2026 TFMX190A03 7/27/2026 TFMX190A04 7/27/2026 TFMX191A04 7/28/2026 TFMX191B04 7/28/2026 TFMX192A01 7/29/2026 TFMX192A02 7/29/2026 TFMX195A04 8/1/2026 TFMX195B03 8/1/2026 TFMX196B02 8/2/2026
Recalling firm:
Taylor Farms de Mexico S. de R.L. de C.V.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 17, 2026

SUBWAY SHRED LETTUCE 1/4" 4/5# Iceberg only products.

Potential Cyclospora contamination.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1283-2026
Lot/product code:
SUBWAY SHRED LETTUCE 1/4" 4/5# TFMX184A01 7/19/2026 TFMX184A04 7/19/2026 TFMX185A01 7/20/2026 TFMX185A03 7/20/2026 TFMX187B03 7/22/2026 TFMX187B04 7/22/2026 TFMX188A04 7/23/2026 TFMX190A02 7/25/2026 TFMX190A03 7/25/2026 TFMX190A04 7/25/2026 TFMX191A04 7/26/2026 TFMX192A09 7/27/2026 TFMX194B03 7/29/2026 TFMX196A02 7/31/2026
Recalling firm:
Taylor Farms de Mexico S. de R.L. de C.V.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 17, 2026

YUM LETTUCE SHREDDED 1/4" 6/5# Iceberg only products.

Potential Cyclospora contamination.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1287-2026
Lot/product code:
YUM LETTUCE SHREDDED 1/4" 6/5# TFMX189A02 7/22/2026 TFMX189A04 7/22/2026 TFMX192A02 7/25/2026 TFMX192A04 7/25/2026
Recalling firm:
Taylor Farms de Mexico S. de R.L. de C.V.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 20, 2026

Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253

Possible Cyclospora Contamination

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1300-2026
Lot/product code:
Best by/Enjoy by dates: 7/13/2026, 7/14/2026/, 7/16/2026, 7/17/2026, 7/18/2026, 7/19/2026, 7/20/2026
Recalling firm:
Piazza Produce (dba CIBUS Fresh)
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 22, 2026

Grade A White In-shell Chicken eggs packaged in the following configurations: 1. Kroger, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 11110-60902 1. Distributed by The Kroger Co., Cincinnati, OH 45202. 2. Kroger, Medium, 30 Eggs, Net Wt 52.5 oz (3lb 4.5oz) 596g, UPC 0 11110-60980 9. Distributed by The Kroger Co., Cincinnati, OH 45202. 3. Kroger, Large 12 Eggs, Net Wt 24 oz (1lb 8oz) 681g, UPC 0 11110-60903 8. Distributed by The Kroger Co., Cincinnati, OH 45202. 4. Kroger, Large 18 Eggs, Net Wt 36 oz (2lb 4oz) 1.03kg, UPC 0 11110-60933 5. Distributed by The Kroger Co., Cincinnati, OH 45202. 5. Kroger, Large 60 Eggs, Net Wt 7lb 8oz (3.40kg), UPC 0 11110-60933 5. Distributed by The Kroger Co., Cincinnati, OH 45202. 6. Kroger, Extra Large 12 Eggs, Net Wt 27 oz (1lb 11oz) 766g, UPC 0 11110-60904 5. Distributed by The Kroger Co., Cincinnati, OH 45202. 7. Kroger, Jumbo 12 Eggs, Net Wt 30 oz (1lb 14oz) 851g, UPC 0 11110-60905 2. Distributed by The Kroger Co., Cincinnati, OH 45202. Packed by Tx Lic #613171, 800 Wabash Rd, N. Manchester, IN 46962. 8. Brookshire's farm fresh, Large 6 Eggs, Net Wt 12 oz (341g), UPC 0 92825-09564 4. Distributed by: Brookshire Grocery Company, P.O. Box 1411, Tyler, TX 75710-1411. 9. Brookshire's farm fresh, Large 12 Eggs, Net Wt 24 oz (1lb 8oz) 681g, UPC 0 92825-09555 2. Distributed by: Brookshire Grocery Company, P.O. Box 1411, Tyler, TX 75710-1411. 10. Brookshire's farm fresh, Large 18 Eggs, Net Wt 36 oz (2lb 4oz) 1.03kg, UPC 0 92825-09556 9. Distributed by: Brookshire Grocery Company, P.O. Box 1411, Tyler, TX 75710-1411. 11. Brookshire's farm fresh, Large 36 Total Eggs TWIN PACK (18 Each), Net Wt 36 oz (2lb 4oz) 1.03kg, UPC 0 92825-10980 8. Distributed by: Brookshire Grocery Company, P.O. Box 1411, Tyler, TX 75710-1411. 12. Super 1 Foods Large 60 Eggs, Net Wt 120 oz (7lbs8oz) 3.4kg, UPC 0 92825-09563 7. Distributed by: Brookshire Grocery Company, P.O. Box 1411, Tyler, TX 75710-1411. 13. Brookshire's farm fresh, Extra Large 18 Eggs, Net Wt 40.5 oz (2lb 8.5oz) 1.15kg, UPC 0 92825-09560 6. Distributed by: Brookshire Grocery Company, P.O. Box 1411, Tyler, TX 75710-1411. 14. Brookshire's farm fresh, Jumbo 12 Eggs, Net Wt 30 oz (1lb 14oz) 851g, UPC 0 92825-09558 3. Distributed by: Brookshire Grocery Company, P.O. Box 1411, Tyler, TX 75710-1411. Packed by MPS Egg Farms, 14374 E State Hwy 21, Byran, TX 77808. 15. Country Morning Medium 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 78566-00104 5. 16. Country Morning Large 12 Eggs, Net Wt 24 oz (1lb 8oz) 681g, UPC 0 78566-20000 4. 17. Country Morning Large 18 Eggs, Net Wt 36 oz (2lb 4oz) 1.03kg, UPC 0 78566-00503 6. 18. Country Morning Large 2 1/2 Dozen Eggs, UPC 0 79307-00516 2. 19. Country Morning Extra Large 12 Eggs, Net Wt 27 oz (1lb 11oz) 766g, UPC 0 78566-00102 1. 20. Country Morning Jumbo 12 Eggs, Net Wt 30 oz (1lb 14oz) 851g, UPC 0 78566-00101 4. 21. Cal-Maine Sunups 2 1/2 Dozen Eggs, UPC 0 28621-30498 7. Packed by Tx Lic #s. 0840962, 0840961 MPS Egg Farms, 2750 County Road 1011, Center, TX 75935. Bulk Product packaged as follows: 22. Medium Grade A JD 183, 15 dozen, MPS Egg Farms TX Lic. No. 0840961, 14374 E Hwy 21, Byran, TX 77808. 23. Medium Grade A JD 158, 30 dozen, MPS Egg Farms TX Lic. No. 0840961, 14374 E Hwy 21, Byran, TX 77808. 24. Large Grade A JD 193, 15 dozen, MPS Egg Farms TX Lic. No. 0840961, 14374 E Hwy 21, Byran, TX 77808. 25. Large Grade A JD 193, 30 dozen MPS Egg Farms TX Lic. No. 0840961, 14374 E Hwy 21, Byran, TX 77808. 26. Grade A Large Egg JD 208, 900 dozen, Distributed by MPS Egg Farms, 14374 E Hwy 21, Byran, TX 77808. 27. Extra Large Grade A, JD 193, 15 dozen, MPS Egg Farms TX Lic. No. 0840961, 14374 E Hwy 21, Byran, TX 77808. 28. Jumbo Grade A, JD 175, 16.67 Dozen, MPS Egg Farms TX Lic. No. 0840961, 14374 E Hwy 21, Byran, TX 77808. Keep Refrigerated at or Below 45-Degrees F.

Possible Salmonella Enteritidis

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1230-2026
Lot/product code:
Code information is printed on the left or right sides of the carton. Codes P-1950 or 0840962 with a Julian Date between 157 and 184 and a Best By/Sell By date Between July 20 - August 17, 2026
Recalling firm:
MIDWEST POULTRY SERVC C/O H & LELECTRIC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 22, 2026

Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes (10lbs, 40lbs, 35lbs, 20lbs, 38lbs 1 1/9 Bushel) ; Product of MX; Coast Tropical TX UPCs 73296608113; 73296600558; 73296610927; 73296600559; 732966107055; 02060042710

Potential Salmonella Javiana contamination

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1242-2026
Lot/product code:
No lot code information. Recall is for all product with a pack date of 07/01/2026 through 07/31/2026
Recalling firm:
Coast Citrus Distributors
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled July 22, 2026

Grade A Brown In-shell Chicken eggs packaged in the following configurations: 1. Simple Truth, Natural Cage Free Grain Fed, Medium, 12 Eggs, Net Wt 21 oz (1lb 5oz) 596g, UPC 0 11110-87032 0. Distributed by The Kroger Co., Cincinnati, OH 45202. 2. Simple Truth, Natural Cage Free Grain Fed, Large, 12 Eggs, Net Wt 24 oz (1lb 8oz) 681g, UPC 0 11110-79770 4. Distributed by The Kroger Co., Cincinnati, OH 45202. 3. Simple Truth, Natural Cage Free Grain Fed, Large, 18 Eggs, Net Wt 36 oz (2lb 4oz) 1,031g, UPC 0 11110-89310 9. Distributed by The Kroger Co., Cincinnati, OH 45202. 4. Simple Truth, Natural Cage Free Grain Fed, Large, 24 Eggs, Net Wt 48 oz (3lb) 1,360g, UPC 0 11110-15097 4. Distributed by The Kroger Co., Cincinnati, OH 45202. 5. Grade A CFB Large Egg, Bulk - BROWN, TICTAC, 900 doz, Distributed by MPS Egg Farms 14374 E State Hwy 21, Byran, TX 77808. Keep Refrigerated.

Possible Salmonella Enteritidis

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1229-2026
Lot/product code:
Code information is printed on the left or right sides of the carton. Codes P-1950 or 0840962 with a Julian Date between 157 and 184 and a Best By/Sell By date Between July 20 - August 17, 2026
Recalling firm:
MIDWEST POULTRY SERVC C/O H & LELECTRIC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 24, 2026

Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container, Frozen Premix, Sterile, Rx only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-3508-41.

Presence of Particulate Matter

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0787-2026
Lot/product code:
Lot # LD175708, Exp Date: 14-Feb-2027.
Recalling firm:
Baxter Healthcare Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 24, 2026

Papaverine HCl Injection, USP, 60 mg/2 mL (30 mg/mL), packaged in a) 2mL Single-Dose Vial (NDC 0517-4002-01), and b) 25x2mL Single-Dose Vials (NDC 0517-4002-25), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.

Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0800-2026
Lot/product code:
Lot #: 25202, Exp. Date: 11/30/2026.
Recalling firm:
American Regent, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 31, 2026

Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution, Manufactured by: Liebel-Flarsheim Company LLC, Raleigh, NC 27616, Made in USA, NDC 0019-1333-65.

Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0773-2026
Lot/product code:
Lot # 25ZF3670, Exp Date: May 31, 2027.
Recalling firm:
Liebel-Flarsheim Company LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 4, 2026

Morphine Sulfate Injection, USP, 2 mg /mL, 1 mL single-dose Simplist prefilled syringes, For Intramuscular or Intravenous use, Rx only, Fresenius Kabi, Lake Zurich, IL. Unit of Use NDC Number 76045-004-01; Unit of Sale NDC Number 76045-004-11

Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0788-2026
Lot/product code:
Lot #: 6402820, Exp. Date 12/2028
Recalling firm:
Fresenius Kabi USA, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 10, 2026

Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, Illinois, 60047, NDC 65219-594-20.

Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0827-2026
Lot/product code:
Lot: 16UI07, Exp 08/31/2028
Recalling firm:
Fresenius Kabi USA, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 12, 2026

Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00

Presence of Particulate matter.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0832-2026
Lot/product code:
Lot#: J4H077, Exp 30NOV2026.
Recalling firm:
B BRAUN MEDICAL INC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 25 mcg, packaged in a) 100-count bottles (NDC 60793-850-01) and b) 1000-count bottles ( NDC 60793-850-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened..

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-251-2013
Lot/product code:
Lot # a) 66675B, Exp. 10/13; b) 66852B Exp. 10/13; 67138B, Exp. 02/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 150 mcg, packaged in a) 100-count bottles (NDC 60793-858-01) and b) 1000-count bottles ( NDC 60793-858-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-259-2013
Lot/product code:
Lot # a) 66375B, Exp. 10/13; 66719B, Exp. 01/14; b) 66904B, Exp. 01/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 112 mcg, packaged in a) 100-count bottles (NDC 60793-855-01) and b) 1000-count bottles ( NDC 60793-855-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-256-2013
Lot/product code:
Lot # a) 67343B, Exp. 01/14; b) 66902B, Exp. 12/13
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 200 mcg, packaged in a) 100-count bottles (NDC 60793-860-01) and b) 1000-count bottles ( NDC 60793-860-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-261-2013
Lot/product code:
Lot # a) 66671B, Exp. 11/13; 67512B, Exp. 02/14 b) 66739B Exp. 11/13; 67513B Exp. 02/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 137 mcg, packaged in a) 100-count bottles (NDC 60793-857-01) and b) 1000-count bottles ( NDC 60793-857-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-258-2013
Lot/product code:
Lot # a) 67013B, Exp. 01/14; b) 66900B, Exp. 01/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 175 mcg, packaged in a) 100-count bottles (NDC 60793-859-01) and b) 1000-count bottles ( NDC 60793-859-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-260-2013
Lot/product code:
Lot # a) 67507B, Exp. 02/14; b) 67508B, Exp. 02/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 50 mcg, packaged in a) 100-count bottles (NDC 60793-851-01) and b) 1000-count bottles ( NDC 60793-851-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-252-2013
Lot/product code:
Lot # a) 66730B, 66853B, Exp. 01/14; b) 66731B, 67116B, Exp. 11/13, 66856B, Exp. 12/13; 67341B, Exp, 02/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 88 mcg, packaged in a) 100-count bottles (NDC 60793-853-01) and b) 1000-count bottles ( NDC 60793-853-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened..

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-254-2013
Lot/product code:
Lot # a) 66619B, Exp. 11/13; 67010B, Exp. 01/14; b) 66733B, Exp. 11/13; 67441B, Exp. 01/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 125 mcg, packaged in a) 100-count bottles (NDC 60793-856-01) and b) 1000-count bottles ( NDC 60793-856-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-257-2013
Lot/product code:
Lot # a) 66373B, Exp. 10/13; 66851B, Exp. 12/13; b)66792B, Exp. 12/13; 67349B, Exp. 03/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 75 mcg, packaged in a) 100-count bottles (NDC 60793-852-01) and b) 1000-count bottles ( NDC 60793-852-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-253-2013
Lot/product code:
Lot # a) 66369B, Exp. 10/13; 66679B, Exp. 11/13; 66850B, Exp. 12/13; b) 66676B, 66732B, Exp. 12/13; 67136B, Exp. 03/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugChemicalRecalled March 28, 2013

Levoxyl (levothyroxine sodium) tablets, USP 100 mcg, packaged in a) 100-count bottles (NDC 60793-854-01) and b) 1000-count bottles ( NDC 60793-854-10 ) Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620.

Chemical contamination: emission of strong odor after package was opened..

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-255-2013
Lot/product code:
Lot # a) 66897B, Exp. 12/13; b) 67137B, Exp.02/14
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2013

Guanabenz 20 mg/ml Injection, compounded by Olympia Pharmacy, Orlando, FL

Not guaranteed to be germ-free: FDA inspection findings resulted in concerns regarding quality control processes

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-738-2013
Lot/product code:
A0422 Exp 7/31/13
Recalling firm:
Lowlite Investments, Inc. D/B/A Olympia Pharmacy
View official FDA record (opens in a new tab)