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.
3,084 stored notices name Connecticut, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.
Reported Aug 10, 2016
ONLINE TDM Vancomycin 100 tests; ONLINE TDM Vancomycin 200 tests; Hitachi Vancomycin (Modular P); Hitachi Vancomycin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2016
Horizon 24 Large Titanium Clips with Adhesive Backing, Ref 004204, Rx Only, Sterile. The metal ligating clips are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Aug 10, 2016
Zimmer¿ Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimmer Air Dermatome II handpiece and width plates…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2016
Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 3, 2016
Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is a homogeneous enzyme immunoassay intended for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2016
Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip, 22 mm, 28 mm, and 32 mm. Non Sterile Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Aug 3, 2016
AUTOCOMP6 XPS High Speed Compounder REF 58810
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Metrix Company
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Frozen Organic Premium Sweet Baby Peas, Organic by Nature brand, net wt. 5 lb. The UPC is 8 46358 00063 3. Frozen IQF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CRF Frozen Foods, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSL Behring GmbH
FDA (openFDA device enforcement)
Reported Jul 27, 2016
ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg Company
24 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
Navitas Naturals Superfood Hemp bar: Creamy Peanut, Hemp, Nut Bar. Net Wt. 1.4 oz/40 G. Gluten free. Ingredients:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Navitas, LLC.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
RayStation 3.0, RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7 and RayStation 5 --- Radiation Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 27, 2016
OT1000 Series Orthopedic Surgical Tables
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jul 27, 2016
AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2016
HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each disposable probe is packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Dehydrated chipotle powder from Silva International packaged in a 50 lb. poly-lined cardboard box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Silva International Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2016Updated Oct 23, 2026
U.S. Cado Holdings, Inc. Recalls Imported Siluriformes Fish Products Distributed Without Meeting FSIS Requirements
High riskUsing this product could cause serious injury, illness or death — stop using it now.U.S. Cado Holdings, Inc.
USDA FSIS
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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.