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.
2,512 stored notices name Mississippi, reported between Jun 20, 2012 and Nov 18, 2026.
Reported Aug 12, 2020
Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sutter Medizintechnik GmbH
FDA (openFDA device enforcement)
Reported Aug 12, 2020
Salmon cut and packaged in Styrofoam case approximately 19 kg per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Topway Enterprises, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 5, 2020
ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2020
FSIS Issues Public Health Alert for Ready-to-Eat Meat and Poultry Products Containing FDA-Regulated Onions that have…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Taylor Farms TX, Inc.
USDA FSIS
Reported Aug 5, 2020
Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Ablation Galil Technology, IcePearl 2.0 CX 90 Cryoablation Needle, Prescription Only Galil Medicals 2.1 CX Cryoablation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Thora-Para 5 Fr Non-Valved Catheter Drainage Tray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2020
Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The IPC system is indicated for the incision/cutting removal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2020
BodyGuard BodySet, REF: A120-160SAS
High riskUsing this product could cause serious injury, illness or death — stop using it now.CME America, LLC
36 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2020
This is an accessory to Intelect Advanced, Intelect Mobile, Intelect Neo, and V-Sonic devices. NYLATEX WRAP - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
FDA (openFDA device enforcement)
Reported Jul 22, 2020
***KIND HEALTHY GRAINS***Oats & Honey Granola with Toasted Coconut***INGREDIENTS: Oats, tapioca syrup, brown rice, cane…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kind LLC
FDA (openFDA food enforcement)
Reported Jul 22, 2020
ACUMED CALLOS INJECT 10CC. Product Number: 65-0010-S, UDI: 813845020245 - Product Usage: Callos is indicated to fill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skeletal Kinetics, LLC
44 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Tecfidera (dimethyl fumarate) delayed-release capsules, 240 mg, 60-count bottle, Rx only, Manufactured by: Biogen Inc.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Biogen MA Inc.
FDA (openFDA drug enforcement)
Reported Jul 15, 2020
EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
Blood gases (PCO2, PO2) and blood pH test system; ABL800 FLEX; Model Number 393-800; UDI (01)05700693938004. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2020
PORT-A-CATH¿ II POWER P.A.C. Low Profile" system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Flow Coupler Monitor, GEM, Global Excellence Microsurgery, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Simply Nature Sweet Potato Bites, 12oz retail boxes variety pack, Expiration date 4/9/2022. Lot code R20AJ-01A.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Praeger's Sensible Foods Inc.
FDA (openFDA food enforcement)
Reported Jul 8, 2020
NORTH STAR TRADING COMPANY SWEET & SALTY CARAMEL TRAIL MIX NET WT 14OZ (396g) MANUFACTURED FOR YOUR MILITARY EXCHANGES…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flagstone Foods LLC
FDA (openFDA food enforcement)
Reported Jul 8, 2020
ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Pediatric Adjustable Flange Tracheostomy Tube Cuffless
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2020
Gordon Choice Imitation Crab Supreme Style, Net Wt 40 oz (2 lb 8 oz) Keep Frozen. UPC 93901-71212. For Distribution…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Trident Seafoods Corporation
FDA (openFDA food enforcement)
Reported Jun 24, 2020
Alinity C, Processing Module. Chemistry analyzer for in-vitro diagnostics.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Jun 24, 2020
PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster
1 more product in this recall
FDA (openFDA device enforcement)
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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.