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Recalls distributed in Pennsylvania

These notices name Pennsylvania 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.

5,819 stored notices name Pennsylvania, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.

Medical devices

Reported Jan 26, 2022

ARIES HSV 1&2 Assay, Part Number/REF 50-10017

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Microbiologics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 19, 2022

Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) cones UPC 4 056489 468646

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lidl US Operations, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Drugs

Reported Jan 19, 2022

Metformin 750 mg Extended Release NDC # 70518-2920-00

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

RemedyRepack Inc.

FDA (openFDA drug enforcement)

Food

Reported Jan 19, 2022

Everything Swapples, Net Wt. 11.14 OZ, UPC 8 64390 00021 3

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Swap Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 12, 2022

Biomeme SARS-CoV-2- Real Time RT-PCR Test, Instructions for Use, Part number 100002824 Subcomponent of: SARS-CoV-2…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomeme, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 12, 2022

Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DiaSorin Molecular LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 12, 2022

QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075); REF 691223

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Drugs

Reported Jan 12, 2022

Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count blister pack (NDC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

RemedyRepack Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 5, 2022

iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

AMO Manufacturing USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomerieux Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 5, 2022

Giant Eagle Diced Green Peppers, 10 oz. 283 g, Frozen bag, 12 packages per case , Best By 10/14/2023 .

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Giant Eagle, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 5, 2022

da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray photon and electron radiation for the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Acclarent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Malosa Core LASIK Pack 2-Medical Refractive Kit- intended to be used to aid in cataract, corneal, or refractive…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beaver Visitec International, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Skinny Needle with Chiba Tip. RPN 090010, 090010-ET; GPN G14254, G15290. Rigid needle available with EchoTip to provide…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Leica Microsystems M220 F12 Microscope Systems

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

FDA (openFDA device enforcement)

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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.