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Recalls distributed in Connecticut

These notices name Connecticut in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

3,077 stored notices name Connecticut, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.

Medical devices

Reported Dec 24, 2025

Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dsaart LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2025

Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lexunder Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 24, 2025

InPen App, Model/CFN Number: MMT-8061 (Android Users)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rocket Medical PLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Seaspine Orthopedics Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 24, 2025

Chef brand Milk Pan 24cm

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Shata Traders Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2025

Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes, 6/5lb bags per case, foodservice item, master…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

JR Simplot Company

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2025

UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Moonlight Packing Corporation

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2025

Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number:…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Orthofix U.S. LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2025

Stuffed Foods brand Cacio e Pepe Arancini; KEEP FROZEN; For institutional use only; Ready-to-cook; Cook to internal…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Stuffed Foods LLC

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Costco Item# 19927 Kirkland Signature Caesar Salad, refrigerated, packaged in clear plastic clamshell container. The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Costco Wholesale Corporation

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Genepro Protein, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 10, 2025

Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Prime Food Processing LLC.

1 more product in this recall

FDA (openFDA food enforcement)

Meat & poultry

Reported Dec 9, 2025

Ghanaianway Restaurant and Grocery LLC Recalls Fresh Salted Lamb Products Produced Without Benefit of Inspection

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Ghanaianway Restaurant and Grocery LLC

USDA FSIS

Medical devices

Reported Dec 3, 2025

CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dermasensor Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Djo, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

IntelePACS - InteleConnect / TechPortal

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intelerad Medical Systems Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 3, 2025

Nat's Nuts Cinnamon Whiskey Pecans, 4 oz.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nats Nuts LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 26, 2025

MONARCH Bronchoscope. Model Number: MBR-000211-B

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The DxFLEX Flow Cytometer is intended for use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.