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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 Mar 24, 2021

Carestream Dental CS 3600 Single Use Normal Tips, Catalog Number 5941216 - Product Usage: used to record the…

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

Carestream Dental, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 24, 2021

Market District Gourmet Pretzel Gift Bag PLU 45505 Net Wt 9 oz Market District Gourmet Pretzel Platter PLU 25206 Net Wt…

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

Giant Eagle

FDA (openFDA food enforcement)

Food

Reported Mar 24, 2021

Tahina Sesame Paste packaged in 1lb and 2lb plastic jars and 10kg metal containers; UPC CODES 6215000382207

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

Kareem Mart Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 24, 2021

Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10oz bottles; and Electrolit Fruit Punch 6 Pack, 625mL/21 oz;…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Laboratorios Pisa Sa De Cv

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 24, 2021

RNA MEDICAL, QCHGB HEMOGLOBIN CONTROL, MULTI, REF QC HGB - Product Usage: monitoring the performance of Hemocue…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 24, 2021

HeartSpan Transseptal Needles Catalog No. FND-019-01, Lot No. E1913644 consisting of an outer needle cannula and an…

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

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire…

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

Getinge Group Logistics America, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer.

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

Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 17, 2021

Hu***CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES***Net Wt. 4 oz (113g); packaged in a black bag; Distributed by: Hu…

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

Hu Products

FDA (openFDA food enforcement)

Medical devices

Reported Mar 17, 2021

Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated…

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

Medical Components, Inc. dba MedComp

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular Ultrasound Catheter is a component of the ACIST…

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

Acist Medical Systems

FDA (openFDA device enforcement)

Drugs

Reported Mar 10, 2021

Famotidine Tablets USP 40mg, 1,000-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc. 279…

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

Aurobindo Pharma USA Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 10, 2021

The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible w/Short Stem Pessary, REF MXKPGSS2-1/4, 2-1/4"…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no…

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

Hamilton Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the…

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/…

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

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 3, 2021

Panang Curry Sauce, 12 fl. oz. (355ml), UPC code #643558406711

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

Barbara's Orchard/Delicae Gourmet

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 3, 2021

Infusion Pump

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover…

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

Ecolab Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 3, 2021

HOUSE AUTRY TARTAR SAUCE NET WT 9 OZ (255g) DISTSRIBUTED BY House -Autry Mills, Inc. Four Oaks, NC 27524 UPC 0 73484…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

House-Autry Mills, Inc.

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.