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 48,100 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.
Reported Aug 4, 2021
Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sunrise Medical (US) LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-12-711, Left Sz. 11 12mm, CE0086, Sterile H2O2, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 28, 2021
Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 21, 2021
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
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)
Reported Jul 21, 2021
Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Owen Mumford USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Beech-Nut brand Single Grain Rice Baby Cereal; NET WT. 8 OZ (227g); INGREDIENTS: Rice flour, sunflower lecithin;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beechnut Nutrition
FDA (openFDA food enforcement)
Reported Jul 14, 2021
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Heart Valves Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
Access SARS CoV-2 lgG II Reagent, REF: C69057, IVD CE UDI: (01)15099590742744
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
GE Healthcare Innova IGS 3 (GTIN 00840682147378), Innova IGS 5 (GTIN 00840682124621), Innova IGS 6 (GTIN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
BulkFoods.com brand dehydrated chopped celery in 1lb and 5lb plastic bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Natural Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 23, 2021
OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended to provide gross immobilization to the cervical spine. REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04
High riskUsing this product could cause serious injury, illness or death — stop using it now.Avid Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
DeRoyal Pacemaker Tray Pgybk, REF 89-6360.06
High riskUsing this product could cause serious injury, illness or death — stop using it now.DeRoyal Industries Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flexible plastic bags UPC 28400 56520
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc. Headquarters
FDA (openFDA food enforcement)
Reported Jun 16, 2021
Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Normand-Info S.A.S.U.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
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.