Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

5551–5575 of 21589

ModerateFDA (Food)·F-0701-2021·2021-06-30
Favorite Day Peanut Butter Chocolate Trail Mix Recalled for Plastic Pieces
John B. Sanfilippo & Son Inc. is recalling Favorite Day Peanut Butter Chocolate Trail Mix because some packages may contain stringy pieces of flexible plastic.
Product
favorite day peanut butter chocolate Trail Mix, Product Number 04315. Peanut butter cups, Milk Chocolate-covered cereal squares, peanuts, chocolate chips and Peanut Butter Chips. Net Wt 8 oz. (226g), UPC 85239-15683
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1942-2021·2021-06-30
Blood Glucose Test Strips Recalled for Temperature Exposure During Shipping
Cardinal Health is recalling ACCU-CHEK SMARTVIEW 100 test strips distributed in Florida, Georgia, and South Carolina due to temperature excursions during shipping that may cause inaccurate glucose readings.
Product
ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0705-2021·2021-06-30
Ful-Flav-R Green Pace Chili Recalled for Plastic Contamination
Pacific Meridian Group is recalling Ful-Flav-R Green Pace Chili Diced due to reports of plastic pieces found in the product. The affected items were distributed in Texas.
Product
Ful-Flav-R Green Pace Chili Diced 3/8" w Citric Acid; Item # 544-107-7 Net Weight 400 lbs. (181.436 KG) Refrigerate after opening. Ingredient: Green Pace Peppers & citric Acid. Ful-Flav-R Products, a Division of Pacific Farms, Oakland, CA 94621
Category
Food
Distribution
1 state
ModerateFDA (Devices)·Z-1935-2021·2021-06-30
Vicks vaporizers recalled for temperature exposure during shipping
Cardinal Health is recalling Vicks 1.5-gallon vaporizers exposed to temperature excursions during shipping delays in February-March 2021, which may cause inaccurate results. Affected units were distributed in Florida, Georgia, and South Carolina.
Product
VAPORIZER VICKS 1.5GAL Item Number: 2354942
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0704-2021·2021-06-30
Dietary supplement Tight! Xtreme Reloaded recalled for unapproved ingredient
SAN Corporation is recalling Tight! Xtreme Reloaded dietary supplement capsules because FDA inspection found an unapproved New Dietary Ingredient, Hordenine, in the product.
Product
Tight! Xtreme Reloaded: 120 count capsules (serving size 3 capsules) Ingredients: Evapor8 Total Body Fat Assault Matrix (Sulbutiamine, Caffeine Anhydrous, Beta-Phenethylamine, Hordeum Vulgare [Root] [Std. to 98% Hordenine], FucoPure [10% Fucoxanthin], Peganum Hamala Extract,
Category
Food
Distribution
4 states
ModerateFDA (Devices)·Z-1945-2021·2021-06-30
Medical Action Industries Hemostats Recalled for Flaking Metal Defects
Medical Action Industries is recalling Mosquito Hemostats due to potential flaking metal and brown spots on the devices. The recall affects 23 boxes of surgical instruments distributed nationwide.
Product
Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1909-2021·2021-06-30
Elastic Poly Probe Cover lacks required FDA 510k clearance
Exact Medical Manufacturing is recalling 17,545 units of a 6" x 48" Elastic Poly Probe Cover that lacks FDA 510(k) clearance for use in body openings. The product should not be used without proper FDA pre-market approval.
Product
6" x 48" Elastic Poly Probe Cover, T Tip,Tele Fold, 2 bands Item ID: A-AU-0852NA
Category
Medical Device
Distribution
6 states
ModerateFDA (Food)·F-0702-2021·2021-06-30
Favorite Day Caramel Cashew Trail Mix Recalled for Plastic Contamination
John B. Sanfilippo & Son Inc. is recalling Favorite Day Caramel Cashew Trail Mix nationwide because the product may contain stringy pieces of flexible plastic.
Product
favorite day caramel cashew Trail Mix, Product Number 04312. Milk Chocolate caramel balls, cashews, M&M'S milk chocolate candies and Peanuts. Net Wt 14 oz. (396g), UPC 85239-15671
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1922-2021·2021-06-30
Ultrasonic Transducer Probe Covers Recalled Due to Missing FDA Clearance
Exact Medical Manufacturing recalled 36,000 ultrasonic transducer probe covers due to missing FDA 510k premarket notification clearance. The affected units were distributed to Florida, Montana, New York, Ohio, Georgia, and Puerto Rico.
Product
Probe Cover 6"x48"- Ultrasonic Transducer Cover Item ID: SH29
Category
Medical Device
Distribution
6 states
ModerateFDA (Food)·F-0706-2021·2021-06-30
Larsen's Creamery Bulk Salted Butter Recall for Pasteurization Defect
Larsen's Creamery, Inc. is recalling Bulk Salted Butter, item #502, due to an out-of-compliance HTST (High Temperature Short Time) recording chart. The recalled butter was made from pasteurized milk on 4/7/21 and distributed in Oregon and Washington.
Product
Bulk Salted Butter, item #502. Butter solid block is packaged in carton case with plastic liner, net wt. 55 lb. (25kg). The label is read in parts: "***BUTTER 55.115 LBS. NET (25 KG) ***PLANT NO. 41-41***".
Category
Food
Distribution
2 states
ModerateNHTSA·21V475000·2021-06-25
Forest River Recalls 2021 East to West Entrada Motorhomes for Placard Error
Forest River is recalling 2021 East to West Entrada motorhomes because the federal placard incorrectly lists six seat belts instead of four, potentially leaving passengers unsecured.
Product
EAST TO WEST — EAST TO WEST ENTRADA
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0629-2021·2021-06-23
Dr. Reddy's Atorvastatin Calcium Tablets Recalled for Failed Impurity Specifications
Dr. Reddy's Laboratories is recalling Atorvastatin Calcium Tablets USP 10 mg nationwide because certain lots contain impurities that exceeded acceptable specifications.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0631-2021·2021-06-23
Phytonadione Tablets 5 mg Recalled Due to Failed Impurities Specification
AVKARE Inc. is recalling Phytonadione Tablets 5 mg because the impurity degradant D level failed to meet specification. The affected lot was distributed in Los Angeles, California.
Product
Phytonadione Tablets 5 mg, Rx Only, 30 Tablets (3x10) Unit Dose, Manufactured for: AvKARE Pulaski, TN 38478. NDC 50268-661-13
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0632-2021·2021-06-23
QiYu Hand Sanitizer Gel recalled for subpotency
World Source LLC is recalling QiYu Hand Sanitizer Gel (500 mL bottles) distributed to two hospitals in New York because the product is subpotent—meaning it contains less active ingredient than specified.
Product
QiYu Hand Sanitizer Gel, ethanol, 500 mL bottles (pump), Manufacturer Guangzhou Minghui Cosmetics Co., Ltd., Baiyun District, Guanzhou
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-1865-2021·2021-06-23
ACUVUE VITA soft contact lenses recalled for potentially incomplete packaging seals
Johnson & Johnson Vision Care is recalling certain ACUVUE VITA soft contact lenses due to potential incomplete packaging seals. Only a limited number of packages from LOT # BOOWWWL are affected.
Product
ACUVUE VITA soft (hydrophilic) contact lens (spherical) for daily wear. Base Curve 8.8, Refractive Power -1.50
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0648-2021·2021-06-23
Ketamine HCl Injection Solution Recalled for Labeling and Expiration Date Errors
Prisma Health Outsourcing Facility is recalling Ketamine HCl Injection Solution (10 mg / 2 mL) distributed in South Carolina due to incorrect expiration dates and incorrect Beyond Use Dates (BUD) on the labeling.
Product
Ketamine HCl Injection Solution, 10 mg / 2 mL (5 mg/mL), Rx Only, Compounded by Prisma Health Outsourcing Facility 1071 Holland Rd. Suite 2 Simpsonville, SC 29681. NDC: 73463-0100-01
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0604-2021·2021-06-16
DELFLEX Peritoneal Dialysis Solution Recall for Temperature Exposure
Fresenius Medical Care is recalling DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose (5000 mL bags, 2-pack) due to temperature abuse during storage or transport that may have compromised product integrity.
Product
DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, 5000 mL bags, 2-pack, Rx Only, Fresenius Medical Care NA, Waltham, MA 02451, NDC 49230-0188-50
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1830-2021·2021-06-16
VIA Microcatheter shipped with incorrect international labeling instead of US labels
MICROVENTION INC. is recalling VIA Microcatheter units that were inadvertently shipped with international labeling instead of US-cleared labeling. Units were distributed in six U.S. states.
Product
VIA Microcatheter VIA 27 REF VIA-27-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0662-2021·2021-06-16
Glaceau Vitaminwater XXX mislabeled; may contain sugar instead of zero sugar
The Coca-Cola Company is recalling Glaceau Vitaminwater XXX acai-blueberry-pomegranate labeled as zero sugar because an incorrect label was used and the product may actually contain sugar.
Product
Glaceau Vitaminwater XXX labeled to be Glaceau Vitaminwater Zero Sugar XXX acai-blueberry-pomegranate, 16.9 FL OZ, made for glaceau, Atlanta, GA
Category
Food
Distribution
12 states
ModerateFDA (Drugs)·D-0610-2021·2021-06-16
DELFLEX Peritoneal Dialysis Solution Recalled for Temperature Abuse
Fresenius Medical Care is recalling 285 cases of DELFLEX Peritoneal Dialysis Solution nationwide because the product was exposed to temperatures outside specified limits during distribution.
Product
DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0658-2021·2021-06-16
Concentrated Creamy Alfredo Sauce recalled for non-food-grade anti-foamer
Kerry Inc. is recalling Concentrated Creamy Alfredo Sauce (product code 20608306, lot 4771420) because it was made with a non-food-grade anti-foamer ingredient.
Product
Concentrated Creamy Alfredo Sauce. Product code 20608306. Keep Frozen. Net Wt. 40 lb. (18.14KG) Distributed By: Kerry Inc., Beloit, WI 53511.
Category
Food
Distribution
5 states
ModerateFDA (Food)·F-0657-2021·2021-06-16
Garlic Alfredo Sauce Recall Due to Non-Food Grade Anti-Foamer
Kerry Inc. is recalling Garlic Alfredo Sauce (product code 20607981) because the product was manufactured with a non-food grade anti-foamer ingredient. The affected sauce was distributed to AZ, CO, OK, TX, and WI.
Product
Garlic Alfredo Sauce. Product code 20607981. Keep Frozen. Net Wt. 30 lb. (13.61KG) Distributed By: Kerry Inc., Beloit, WI 53511.
Category
Food
Distribution
5 states
ModerateFDA (Drugs)·D-0624-2021·2021-06-16
READYPREP CHG Chlorhexidine Gluconate Cloth recalled for superpotency
Medline Industries is recalling READYPREP CHG 2% Chlorhexidine Gluconate Cloth because the product contains higher-than-specified levels of the active ingredient.
Product
READYPREP CHG — READYPREP CHG (CHLORHEXIDINE GLUCONATE 2%)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0609-2021·2021-06-16
DELFLEX Peritoneal Dialysis Solution Recalled for Temperature Abuse Exposure
Fresenius Medical Care is recalling DELFLEX Peritoneal Dialysis Solution (Lot #20PU04030, 4 cases) distributed nationwide because the product was exposed to temperatures outside specified limits, which may affect safety and efficacy.
Product
DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0661-2021·2021-06-16
Mideo's Marinara Glass Jars Recalled for Incorrect Potassium Labeling
RC Industries Inc. is recalling Mideo's Marinara Glass 32oz jars because the potassium content listed on the label does not match the actual amount per serving.
Product
Mideo's Marinara Glass 32oz jars - 6 jars per case
Category
Food
Distribution
9 states