Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

22076–22100 of 25981

HighFDA (Devices)·Z-0812-2022·2022-03-30
Biomet Trauma Surgical Instruments Recalled Due to Packaging Defect
Biomet is recalling TRAUMA Drill Bits, Taps, and Guide Pins due to packaging that may not seal properly, potentially compromising sterile barrier integrity and posing a risk of surgical site infection.
Product
BIOMET TRAUMA Drill Bit, Tap, Guide Pin: [DVR Drill Bit, Item # 212000022, DVR 2.2MM DRILL BIT], [ALPS Drill Bit, Item # 214227160, 2.7X160MM CALIBRATED DRILL], [ALPS Drill Bit, Item # 824273100, 4.5X150MM DRILL], [ALPS Drill Bit, Item # 829029170, 2.5X140MM DRILL], [ALPS Drill B
Category
Medical Device
Distribution
28 states
HighFDA (Devices)·Z-0823-2022·2022-03-30
NuOss Collagen Blocks Recalled Due to Product Substitution Error
Ace Surgical Supply is recalling NuOss Collagen Blocks because some units were mistakenly packaged with Collatene Fibrillar Collagen instead, which may result in suboptimal bone repair during dental and maxillofacial procedures.
Product
NuOss Collagen Block Size 8mm x 9mm x 9mm- used in filling periodontal and maxillofacial defects. Catalog Number: 5099250
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0683-2022·2022-03-30
Fluocinonide Cream Recalled for Manufacturing Compliance and Stability Deviations
Teligent Pharma, Inc. is recalling Fluocinonide Cream USP 0.1% due to manufacturing compliance deviations and discontinuation of stability studies. The recall affects products nationwide in the USA and Puerto Rico.
Product
Fluocinonide Cream USP, 0.1%, 120 grams tube, Rx Only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310, NDC 52565-079-11.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0820-2022·2022-03-30
Compella Bariatric Bed System Recall—Power Cord Electrical Shock Risk
Baxter Healthcare is recalling the Compella Bariatric Bed System due to potential power cord damage that could expose electrical conductors, creating a shock hazard. Approximately 5186 units worldwide are affected.
Product
Compella Bariatric Bed System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0908-2022·2022-03-30
Snak Yard Dried Plums Recalled for Potential High Lead Content
Alli & Rose LLC is recalling Snak Yard Dried Plums Saladitos due to potential high lead content. Affected products were distributed in California with best-before dates of February 14, 2023, or April 29, 2023.
Product
Snak Yard Dried Plums Saladitos; 12.7 oz. net wt (360g) Item number 1546905 UPC: 8 10019 60082 1 Made in China; Packed in Thailand Distributed by Alli & Rose LLC, 1422 E, ?M?ain St. PMB #210 Lincolnton NC 28092
Category
Food
Distribution
1 state
HighFDA (Food)·F-0902-2022·2022-03-30
PB Choc Protein Bites Recalled for Undeclared Coconut Allergen
HumbleHungryHappy LLC is recalling PB Choc Protein Bites because coconut is not listed in the allergen declaration, posing a risk to consumers with coconut allergies.
Product
PB CHOC PROTEIN BITES, net wt. 7.2 oz. There are 6 bites in a rectangular flexible plastic clamshell covered with plastic film lid. Product label is read in parts: "***PB CHOC PROTEIN BITE***Ingredients: Peanut Butter, Coconut Milk, Orgain Organic Protein, Hershey Semi-Sweet
Category
Food
Distribution
1 state
HighFDA (Food)·F-0897-2022·2022-03-30
Flow Alkaline Spring Water Recalled Due to Alleged Adverse Reactions
Flow Beverages Inc. is recalling Flow Alkaline Spring Water (Organic lemon & ginger, 500 ml) due to four customer complaints of alleged adverse reactions. Affected lots are 2023AUG29 V5, distributed to eleven states.
Product
Flow Alkaline Spring Water - Organic lemon & ginger flavored water. 500 ml unit . Tetra Pak paper carton.
Category
Food
Distribution
11 states
HighFDA (Food)·F-0906-2022·2022-03-30
Thai Noodle Salad Kits recalled for potential foreign material contamination
Pacific Coast Fruit Company is recalling Kit Thai Noodle Salad FM due to potential foreign material in an ingredient. The product was distributed to retailers in Alaska, Idaho, Oregon, and Washington.
Product
Kit Thai Noodle Salad FM; Net weight 6.75 lbs. UPC 0-20728-72698-0. Product is RTE, refrigerated, ready to mix by the retailer for sale at the retail store. Product comes in a kit that contains Thai Noodle Salad Base (recalled by Fresh Creative Foods; RES 89741), brussels/carrot
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-0809-2022·2022-03-30
Biomet Surgical Implant Reamer Recall: Packaging Sterile Barrier Risk
Biomet is recalling surgical implant reamers due to packaging that may lose sterile barrier integrity, risking post-surgical infection.
Product
BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373, 8MM], [Item #110018275, 5MM]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels.
Category
Medical Device
Distribution
28 states
HighFDA (Devices)·Z-0821-2022·2022-03-30
Medical Device Air Supply Unit Recalled for Potential Electrical Shock Hazard
Baxter Healthcare is recalling the Compella Therapy Air Supply Unit due to potential power cord damage that could expose electrical conductors and create a shock risk. The recall affects 6,022 units distributed worldwide.
Product
Compella Therapy Air Supply Unit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0681-2022·2022-03-30
Diflorasone Diacetate Ointment recalled due to discontinued stability studies
Teligent Pharma is recalling all unexpired Diflorasone Diacetate Ointment 0.05% due to cGMP deviations. The company discontinued its stability study program, preventing verification that the product maintains safety and effectiveness throughout shelf life.
Product
Diflorasone Diacetate Ointment USP, 0.05%, Net Wt 60 g tubes, Rx only, Manufactured for: SOLA Pharmaceuticals, LLC Baton Rouge, LA 70809, NDC 70512-031-60.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0810-2022·2022-03-30
BIOMET Trauma DVR CROSSLOCK implants recalled for packaging integrity
BIOMET Trauma DVR CROSSLOCK surgical implant plates may have packaging that does not maintain sterile barrier integrity, posing a risk of infection.
Product
BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # 1318-12-126, DVR CROSSLOCK EXTRA LONG PLATE RIGHT], [Item # 1318-12-176, DVR CROSSLOCK EXTRA EXTRA LONG PLATE RIGHT]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton
Category
Medical Device
Distribution
28 states
HighFDA (Devices)·Z-0734-2022·2022-03-30
Azurion Medical Imaging System Software Defect Affects Patient Dose Control
Philips Azurion R2.1 systems have a software defect that causes the Patient Type to change unexpectedly when starting a procedure, potentially affecting dose control settings without user notification.
Product
Azurion systems with software release R2.0.x
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0811-2022·2022-03-30
Biomet Fibula Composite Locking Plate Recall Due to Sterile Barrier Packaging Defect
Biomet is recalling TRAUMA A.L.P.S. fibula composite locking plates due to packaging that may not maintain sterile barrier integrity, posing a risk of infection if used.
Product
BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.
Category
Medical Device
Distribution
28 states
HighFDA (Drugs)·D-0706-2022·2022-03-30
Norepinephrine Bitartrate Injection Recalled Due to Defective Container
Athenex Pharma Solutions is recalling Norepinephrine Bitartrate Injection due to defective containers affecting specific lots distributed nationwide.
Product
Norepinephrine Bitartrate Injection 4mg per 250 mL in 0.9% Sodium Chloride, 4 mg, 250 mL excel bag, Rx only, Athenex Pharma Solutions, LLC, Clarence, NY, 14031, NDC 76154-474-15
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0669-2022·2022-03-30
FDA Recalls Betamethasone Dipropionate Lotion Due to Manufacturing Deviations
Teligent Pharma is recalling Betamethasone Dipropionate Lotion due to manufacturing practice deviations and discontinuation of the stability study program. The recall affects 43,218 bottles distributed nationwide.
Product
Betamethasone Dipropionate Lotion USP, 0.05%* (Augmented), packaged in a) 30 mL (29 grams) bottles, NDC 52565-023-29; b) 60 mL (58 grams) bottles, NDC 52565-023-59, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0818-2022·2022-03-30
Codman Cranial Access Kits Recall: Incorrect Expiration Dates on Labels
Integra LifeSciences is recalling Codman Cranial Access Kits due to incorrect extended expiration dates printed on outer box labels. Using expired kits may result in pain, infection, or adverse tissue reaction.
Product
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Part Number: 826616
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0899-2022·2022-03-30
Damascus Bakery Bantam Classic Bagels Recalled for Undeclared Egg Allergen
Damascus Bakery is recalling Bantam Classic Bagels due to undeclared egg allergen. Affected product was distributed to SC, PA, MA, MN, NY, and IN.
Product
Damascus Bakery, Bantam Classic Bagels, 6/1.3 oz pieces per carton (7.8 oz), Paper Carton .
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0813-2022·2022-03-30
Outset Tablo Hemodialysis Console Recalled for Heat Damage Risk
Outset Medical is recalling Tablo hemodialysis consoles (models PN-0003000 and PN-0006000) nationwide due to a component that may cause heat-related damage to the device.
Product
Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0900-2022·2022-03-30
Shredded Cheese Recalled for Potential Metal Contamination
Schreiber Foods is recalling shredded cheese due to potential metal contamination. No illnesses have been reported.
Product
Shredded Cheese consisting of Monterey Jack, Queso Quesadilla, and Asadero cheeses, Net Wt 2lbs, packaged in plastic pouches, 12 pouches per case.
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-0817-2022·2022-03-30
Codman Cranial Access Kits Recalled Due to Incorrect Expiration Dates on Labels
Integra LifeSciences is recalling 1,161 Codman Cranial Access Kits due to incorrect expiration dates on the outer box labels. Using the product past its correct expiration date may cause pain, infection, or adverse tissue reaction.
Product
Codman Cranial Access Kits- indicated when a craniotomy is required for placement of an intracranial pressure (ICP) monitoring device and/or cerebrospinal fluid drainage procedures. Product umber: 826614
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0901-2022·2022-03-30
Overnight Oats Recall: Undeclared Almond and Coconut Allergens
HumbleHungryHappy LLC is recalling Overnight Oats due to undeclared almond and coconut allergens on the label. Consumers with allergies to these ingredients face potential health risks.
Product
Overnight Oats, net wt. 9.4 oz. It is packaged in flexible plastic bowl with film lid. Product label is read in parts: "***OVERNIGHT OATS***Ingredients: 1% Greek Yogurt ***Coconut Milk, Orgain Organic Protein, Rolled Oats, Almond, Milk, Honey, Flaxseeds, Coconut***Contains: Mi
Category
Food
Distribution
1 state
HighNHTSA·22V203000·2022-03-29
Travel trailers with defective power inlet bolts risk fire
Grand Design is recalling certain 2022 Reflection and Transcend travel trailers with 50-amp shore power inlets. The power inlet lug bolts may be too hard to tighten properly, creating loose electrical connections that can cause fire.
Product
GRAND DESIGN — 2022 GRAND DESIGN REFLECTION
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V199000·2022-03-29
2022 Heartland North Trail trailers recalled for incorrect weight certification labels
Heartland is recalling 2021-2022 North Trail trailers because the Gross Axle Weight Rating on the federal certification label is incorrect, risking vehicle overloading and crashes.
Product
HEARTLAND — 2022 HEARTLAND NORTH TRAIL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V202000·2022-03-29
2022 Kia Sorento Oil Supply Pipe May Crack, Creating Fire Risk
Kia is recalling certain 2022 Sorento vehicles because the turbocharger oil supply pipe may crack, causing an oil leak that could increase the risk of engine fire.
Product
KIA — 2022 KIA SORENTO
Category
Vehicle
Distribution
Distributed nationwide

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22076–22100 of 25981