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. A further 48,784 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.
Reported Mar 4, 2020
C&H Pure Cane Sugar Golden Brown, 32 oz (2 LB) plastic bag, UPC 015800090038, Lots 50042 (Best By Jan 21, 2022) & 50043…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Domino Foods Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 4, 2020
Coburn Farms Snackers, Sharp Yellow Cheddar Cheese, Cherry Juice Infused Dried Cranberries & Roasted Sea Salted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Great Lakes Cheese Co. Inc.
FDA (openFDA food enforcement)
Reported Mar 4, 2020
Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical, Cardiac Rhythm Management Division
FDA (openFDA device enforcement)
Reported Mar 4, 2020
THP Hip Plating System, Item Nos. 14-451070 14-451075 14-451080 14-451085 14-451090 14-451095 14-451100 14-451105…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Glycopyrrolate Injection, USP 4 mg per 20 mL (0.2 mg/mL), 20 mL Multiple Dose Vial, Rx Only, For Intramuscular or…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.AuroMedics Pharma LLC
FDA (openFDA drug enforcement)
Reported Feb 26, 2020
SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017
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 Feb 19, 2020
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market America Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nextremity Solutions
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
cobas infinity core, Material No. 7154003001. The device is a calculator/data processing module, for clinical use.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Almark Foods, LLC
28 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Reinforced Introducer Sets Maquet 7 Fr., Part Number: 0684 00 0403 06. It is an accessory to be used for percutaneous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
ranitidine hydrochloride, USP ,150 mg tablets a) 14-count bottles ( NDC 43063-844-14); b) 30-count bottles (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PD-Rx Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2020
Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
21 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jeni's Splendid Ice Creams LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
12lb plastic bucket of Egg Salad Sold as 2 - 12lb buckets per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Knotts Fine Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 5, 2020
AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
FDA (openFDA device enforcement)
Reported Feb 5, 2020
RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jan 29, 2020
Morrison's cornbread dressing packaged in 4lb tray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Savannah Food Company, Inc.
5 more products in this recall
FDA (openFDA food 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.