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 Sep 30, 2020
Perceval Single Use Accessory Kit, Size S, REF: ICV1345, Sterile EO, Rx Only, CE, UDI: 8022057015204 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group Italia S.r.l.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Spicy Beef & Vegetables with Rice & Sesame Seeds meal kits containing onions delivered the week of July 27, 2020.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Apron Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 23, 2020
FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot) FLX-290-10; FLX-290-20 and Track to Rack Module…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inpeco S.A.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novarad Corporation
FDA (openFDA device enforcement)
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh US
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Merge PACS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Whole Foods Market Vegan Vanilla Cake 6 Inch NET WT 2lb 11oz (1219g) Packed for Whole Foods Market PLU 41070 packaged…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Sep 9, 2020
BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2020
StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stimwave Technologies Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2020
Pleur-evac Thoracic Catheters Catalog No: DTRC-20S The thoracic catheter is indicated to be used in any surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster (israel), Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neurovision Medical Products Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2020
E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2020
Whole Foods Market Buttermilk Biscuits, 4pk NET WT 1lb 0 oz PLU: 30561 packaged in plastic clam shell
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market
FDA (openFDA food enforcement)
Reported Aug 26, 2020
ClosureFast Micro Introducer Sheath Set, REF MIS-7F11; 7Fr/Ch (2.3mm)x11 cm. STERILE|EO; Rx ONLY - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2020
Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2020
Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smith Foods Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2020
MURRAY'S CHADS SMOKED GOUDA DIP in plastic tubs, all sizes.
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2020
AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Linet Americas
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2020
Leucovorin Calcium Tablets USP, 10 mg, Rx only, 24 Tablets per bottle, Distr. by: West-Ward Pharmaceuticals Corp.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.West-Ward Columbus Inc.
FDA (openFDA drug 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.