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 19, 2026Updated Aug 25, 2026
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OBP Medical Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Sep 14, 2026
Cibus Fresh, Sprig & Sprout, and Jack & Olive brand Garden Salad, 7.75oz clear plastic container, UPC 810028250253
High riskUsing this product could cause serious injury, illness or death — stop using it now.Piazza Produce (dba CIBUS Fresh)
FDA (openFDA food enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
GM Helix Implant, Endosseous Dental Implant Article No. 109.984
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Sep 7, 2026
MARKETSIDE ICEBERG SALAD 10/24 oz, UPC 681131328951; MARKETSIDE ICEBERG SALAD 12/12 oz, UPC 681131328944; MARKETSIDE…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms de Mexico S. de R.L. de C.V.
20 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2026
REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following instruments: -…
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 Aug 12, 2026
Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 SC 240cm Box 20;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 12, 2026
HardyDisk AST Cefiderocol 30¿g (FDC30) REF Z9435 HardyDisk AST Cefiderocol 30¿g (FDC30) for in vitro agar diffusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Aug 12, 2026Updated Sep 16, 2026
Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KAO USA Inc.
FDA (weekly enforcement report)
Reported Aug 12, 2026
Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pride Mobility Products Corp.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026Updated Sep 16, 2026
Immune Globulin (Human); Octagam IVIG 10% 30gm/300mL (Batch KP12B8561)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
FDA (weekly enforcement report)
Reported Aug 5, 2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Permobil Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penumbra, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
SeaSpine Polyaxial Head REF Number: 41-3010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Jul 22, 2026
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2026
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 22, 2026
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix U.S. LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
2 more products 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.