All recall categories

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.

3,041 stored notices name Connecticut, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.

Medical devices

Reported Jul 4, 2018

Single Chamber Temporary External Pacemaker, Model 53401

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

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 4, 2018

RayStation Radiation Therapy Treatment Planning System; 6.0, 6.1, 6.2, 7.0 Product Usage: Usage: RayStation is a…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Food

Reported Jul 4, 2018

Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16…

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

Utz Quality Food Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 4, 2018

Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 27, 2018

Kellogg's Honey Smacks, 15.3 oz. and 23 oz.

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

Kellogg Company

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls (High 125 ng/ml and Low 75 ng/ml) are used as control…

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

Alere San Diego Inc. dba Immunalysis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124

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

Angiodynamics Inc. (Navilyst Medical Inc.)

37 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or…

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

Keystone Dental Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350

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

Philips Electronics North America Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2018

Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz /12 per case, in mylar metalized bag in gable box,

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

R.A.B. Food Group LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

cobas e 801 immunoassay analyzer, cobas 8000 Modular Series The device is a fully automated, software controlled…

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

Roche Diagnostics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

Part #: SAM XT-M, Model: Tactical Black or Military

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

The Seaberg Company Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Broccoli cuts, All Natural, No Preservatives, Net Wt 16 OZ; Distributed by Foodhold USA, LLC, Landover, MD 20785; UPC:…

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

Ahold USA

FDA (openFDA food enforcement)

Food

Reported Jun 13, 2018

Priano Rosso Pesto Sauce, 6.7oz glass jar

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

BLM Products U. Vertriebsges

FDA (openFDA food enforcement)

Food

Reported Jun 13, 2018

Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic package with UPC 4770049011188.

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

Desly International Corp.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…

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

Draeger Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Heritage Shortbreaad Lemon Infused Ingredients: Enriched flour, pasteurized cream(milk),sugar, salt, pure crystallized…

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

Heritage Short Bread, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive…

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

Invivo Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…

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

Lake Michigan Distilling Co. LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Restoris MCK Onlay Insert Extractor.

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Trader Joe's Artisan Bread - Organic French Baguette; (Brown and Serve) Keep frozen; Product code 53835; 24 x 11.5 oz.…

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

Trader Joes Company

FDA (openFDA food enforcement)

Medical devices

Reported Jun 6, 2018

Carina Ventilator, ventilator. Catalog no. 5704110. Long-term ventilator for treatment in hospitals by a qualified…

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

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…

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

Gyrus Acmi, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding…

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

Maquet Datascope Corp. - Cardiac Assist Division

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.