Hazard

Mispackaging recalls

24 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 24
Critical: 0
Severe: 4
Most recent: 2025-12-31

Of the 24 mispackaging recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (17%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mispackaging recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–24 of 24

HighFDA (Devices)·Z-0978-2026·2025-12-31
Ritz peanut butter cracker sandwiches recalled over undeclared peanut from mispackaging
Mondelez Global is recalling 70 cases of Ritz Peanut Butter Cracker Sandwiches over undeclared peanut due to mispackaging.
Product
Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number: 815609380 Software Version: N/A Product Description: Affixus 9 mm, Length 380 mm, Left, Trochanteric Nail Component: N/A
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0349-2025·2025-08-06
Casa Mamita churro bites recalled after cheese stick found in bag
Casa Mamita Churro Bites Filled with Chocolate Hazelnut Cream are being recalled for undeclared milk after a consumer found a breaded halloumi cheese stick in a bag. 19,080 sell units affected.
Product
Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cream, 7.5 oz , Cardboard Box, 12 boxes per case, Keep Frozen Until Ready For Use
Category
Food
Distribution
6 states
HighFDA (Food)·H-0319-2025·2025-07-30
Artisan style half loaves recalled over undeclared hazelnut from mispackaging
Artisan Style 1/2 Loaf white bread is being recalled because product containing hazelnuts was put in bags whose allergen statement does not include hazelnuts. 883 loaves are affected.
Product
Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two splits on top 7/13/2025 - Best By Flexible plastic bag
Category
Food
Distribution
11 states
HighFDA (Food)·H-0324-2025·2025-07-30
Ritz peanut butter cracker 40 count cartons recalled over undeclared peanut
Ritz Peanut Butter Cracker Sandwiches in 55.2 oz 40 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 224 cases are affected.
Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 count (40x1.38 oz 6 pack of cracker sandwiches inside carton. 40 - 55.2oz Cartons in master carton. UPC 0 44000 07819 5
Category
Food
Distribution
49 states
HighFDA (Food)·H-0326-2025·2025-07-30
Ritz peanut butter cracker sandwiches recalled over undeclared peanut from mispackaging
Ritz Peanut Butter Cracker Sandwiches are being recalled because of undeclared peanut allergens due to mispackaging. 37,985 units are affected across nearly every state.
Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton. 14X8-Case: 14 - 11.04 Oz Cartons in master carton. UPC 0 44000 88210 5
Category
Food
Distribution
49 states
HighFDA (Food)·H-0325-2025·2025-07-30
Ritz cracker sandwich variety packs recalled over undeclared peanut from mispackaging
Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.
Product
Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese 1.35 oz Packs and 10 Peanut Butter 1.38 oz Packs) Net Wt. 27.3 oz (20-1.38 oz packet of cracker sandwiches inside cartons of varying sizes). 20-27.3 OZ (Case: 6 - 27.3 Oz Cartons in master carton. UP
Category
Food
Distribution
49 states
HighFDA (Food)·H-0323-2025·2025-07-30
Ritz peanut butter cracker 20 count cartons recalled over undeclared peanut
Ritz Peanut Butter Cracker Sandwiches in 27.6 oz 20 count cartons are being recalled because of undeclared peanut allergens due to mispackaging. 24,446 cases are affected.
Product
Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside cartons. And 6x20(6 - 27.6 oz Cartons) in master carton. UPC 1 00 44000 07584 2
Category
Food
Distribution
49 states
HighFDA (Devices)·Z-1257-2022·2022-06-15
DJO EMPOWR 3D Knee Tibial Insert Mispackaged—Risk of Wrong Implant
Encore Medical is recalling DJO EMPOWR 3D Knee tibial inserts because packages may contain a mismatched left-size component instead of the correct right-size implant. If implanted, the wrong component could leave debris in the joint.
Product
DJO EMPOWR 3D Knee (Right) 10mm Tibial Insert, REF: 342-10-708
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1005-2022·2022-04-20
Back to Nature Cheese Crackers Recalled Due to Undeclared Egg and Milk Allergens
B&G Foods is recalling Back to Nature Cheddalicious Cheese Flavored Crackers due to undeclared egg and milk allergens caused by mispackaging. Consumers with egg or milk allergies should discard the product or return it.
Product
Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case
Category
Food
Distribution
9 states
ModerateFDA (Drugs)·D-0647-2020·2020-01-08
Akorn Recalls Myorisan 20mg Capsules Due to Mispackaging Error
Akorn, Inc. is recalling Myorisan (isotretinoin) 20mg capsules because some cartons contained 40mg blister cards. The error was found in a customer complaint.
Product
MYORISAN (isotretinoin capsules, USP), 20mg, packaged in 30-count Capsules (3 x 10 Prescription Packs) per box, Rx only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forset, IL 60045; NDC 61748-302-13.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1487-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Extended-Release Capsules
Amerisource Health Services is recalling 126 cartons of amphetamine extended-release capsules due to unit dose mispackaging where blister cavities may contain multiple capsules.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 15 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Pa
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1482-2016·2016-09-14
Amerisource Recalls Mispackaged Amphetamine Tablets Due to Unit Dose Errors
Amerisource Health Services is recalling 2,276 cartons of 10 mg amphetamine tablets because blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 10 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1489-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Extended-Release Capsules
Amerisource Health Services is recalling 115 cartons of 25 mg amphetamine extended-release capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 25 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health P
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1485-2016·2016-09-14
Amerisource Recalls Mispackaged Amphetamine Tablets Due to Dosing Errors
Amerisource Health Services is recalling 156 cartons of 30 mg amphetamine tablets because blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 30 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus,
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1484-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Tablets
Amerisource Health Services is recalling 867 cartons of 20 mg amphetamine tablets due to unit dose blister cavities containing more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 20 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus,
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1486-2016·2016-09-14
Amerisource Health Services Recalls Mispackaged Amphetamine Extended-Release Capsules
Amerisource Health Services is recalling 834 cartons of amphetamine extended-release capsules because blister cavities may contain more than one tablet or capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 10 mg 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health P
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1483-2016·2016-09-14
Amerisource Recalls Mispackaged Amphetamine Tablets Due to Unit Dose Errors
Amerisource Health Services is recalling 1,416 cartons of 15 mg amphetamine tablets because blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 15 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1488-2016·2016-09-14
Amerisource Recalls Mispackaged Adderall XR 20 mg Extended-Release Capsules
Amerisource Health Services is recalling 666 cartons of Adderall XR 20 mg capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules, CII 20 mg, 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1490-2016·2016-09-14
Amerisource Recalls Mispackaged Adderall XR 30 mg Extended-Release Capsules
Amerisource Health Services is recalling 761 cartons of Adderall XR 30 mg capsules due to unit dose mispackaging where blister cavities may contain more than one capsule.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Pa
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1481-2016·2016-09-14
Amerisource Recalls Mispackaged Dextroamphetamine and Amphetamine Tablets
Amerisource Health Services is recalling 221 cartons of mixed amphetamine tablets due to unit dose mispackaging, where blister cavities may contain more than one tablet.
Product
Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 5 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1034-2016·2016-03-09
FDA Recalls Mispackaged Pediatric Feeding Tubes from Covidien
The FDA is recalling 1,330 units of pediatric feeding tubes due to packaging errors where different tube sizes were placed in incorrect packages.
Product
Covidien Kangaroo Polyurethane Feeding Tube Radiopaque Line, Safe Enteral Connections 8 Fr/Ch (2.7 mm) x 20" (51 cm); Catalog Number: 461701. Intended for pediatric feeding.
Category
Medical Device
Distribution
1 state
ModerateFDA (Food)·F-2739-2015·2015-07-01
Eating Right Black Bean Soup Recalled for Potential Mispackaging
San Francisco Spice Company is recalling Eating Right Black Bean Soup because some containers may contain Spicy Thai Noodle soup instead.
Product
Eating Right Black Bean Soup; 1.3 oz paper container. Dried soup to which consumer adds hot water. USPC: 79893-80026; Ingredients: Ingredients: Black Beans*, Vegetables* (Tomato, Potato, Corn, Peppers, Garlic), Natural Flavor (Yeast Extract, Maltodextrin, Sunflower Oil, Silicon
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-827-2013·2013-08-07
Procter & Gamble Recalls DayQuil and NyQuil Sinex Liquicaps Due to Packaging Defects
Procter & Gamble is recalling 35,568 cartons of DayQuil and NyQuil Sinex liquicaps nationwide due to packaging defects that may cause missing or misplaced capsules.
Product
DayQuil Sinex DayTime Sinus Relief (acetaminophen 325 mg and phenylephrine HCl 5 mg) liquicaps and NyQuil Sinex NightTime Sinus Relief (acetaminophen 325 mg, doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg) liquicaps Combopack, each 48-count liquicaps per carton contains
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-018-2013·2012-10-31
Bristol-Myers Squibb Recalls Mispackaged Kombiglyze XR Physician Sample Cartons
Bristol-Myers Squibb is recalling 117,049 physician sample cartons of Kombiglyze XR because some external cartons were mislabeled with the wrong dosage, though the individual blister units inside are correctly labeled.
Product
Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets, Physician Sample-Not For Sale, 6 Tablets per Carton, 2.5 mg/1000 mg, Rx only, Manufactured By: Bristol-Myers Squibb Company, Princeton NJ 08543, USA, Marketed By: Bristol-Myers Squibb Company, Princeton NJ 08
Category
Drug
Distribution
Distributed nationwide