Recalls distributed in Mississippi
These notices name Mississippi 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.
2,477 stored notices name Mississippi, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.
Reported Aug 14, 2013
Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole) Product Usage: The Sonopet Console is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 7, 2013
AIA Analyzer Pipette Tips used on Tosoh AIA-2000, AIA-1800, AIA-900 and AIA-600II Analyzers, 1000 tips/bag AIA-Analyzer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Smd Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Endopath Electrosurgery Probe Plus II, twelve (12) different devices, including hooks, spatulas, right angles, curved…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2013
HemosIL RecombiPlasTin 2G, Part Number 0020002950 (8 ml size). The product is used for the evaluation of the extrinsic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory Co.
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Dermalight 80 Model Number UVB-080, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.National Biological Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Rultract Retractor Ratchet Cover Plate Distributed by Pemco, Inc., Cleveland, OH 44131 Surgical retractor used to lift…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pemco Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2013
nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2013
CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Fudge Buttercream Frosted Peanut Butter cookies, some of which were mislabeled by being wrapped in Buttercream Frosted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cheryls
FDA (openFDA food enforcement)
Reported Jul 10, 2013
HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clorox Healthcare Holdings, LLC (dba HealthLink)
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
1) VITROS 5,1 FS Chemistry System (product code 6801375) and 2) VITROS 5,1 FS Chemistry System Refurbished (product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medrad Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Brilliance CT 64, Ingenuity CT, Ingenuity Core, and Ingenuity Core128 scanners are whole body Computed Tomography X-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 3, 2013
Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jun 26, 2013
Lightlife Farmer's Market Veggie Burgers, meat free, 12 oz/4-count bag, packaged in 5/12 oz-bag/cartons. Distributed…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Inc.
FDA (openFDA food enforcement)
Reported Jun 26, 2013
Actiq (oral transmucosal fentanyl citrate) 200 mcg, lozenge on a stick, a)Single Blister (NDC 63459-502-01), b) 30…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA, Inc.
FDA (openFDA drug enforcement)
Reported Jun 26, 2013
GlideScope Video Laryngoscope (GVL) 3, 4, 5 and GlideScope (AVL) 2, 3, 4 and 5 reusable blades Product Usage: The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Verathon, Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2013
XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Atlantic Pro Nutrients, Inc. dba XYMOGEN
FDA (openFDA food enforcement)
Reported Jun 12, 2013
AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Corp.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2013
BrightView SPECT gamma camera for Emission Computed Tomography, Philips Medical Systems, Cleveland, OH 44143 BrightView…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2013
AMBI 15DM/100GFN/5PEH, Antitussive, Expectorant, Nasal Decongestant, Grape Flavor, 4 fl oz. bottle, OTC, Manufactured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TG United, Inc.
43 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 5, 2013
EZ Breathe Atomizer Model # EZ-100. For the delivery of liquid medications for respiratory usage.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nephron Pharmaceuticals Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Mississippi recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.