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.
5,900 stored notices name Pennsylvania, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Pennsylvania too — those are in the archive.
Reported Jul 27, 2016
The TDL Group Corp. Recalls Dried Chicken Soup Mix Products Distributed Without Benefit of Import Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.The TDL Group Corp.
USDA FSIS
Reported Jul 27, 2016
The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
16 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each disposable probe is packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Devicor Medical Products Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
QuickSlide MGS-80, Automated Mutli-Slide Gram Stainer/GramPRO-80. Systematically stains, rinses, decolorizes, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Jul 20, 2016
HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
cobas¿ Liat Influenza A/B Quality Control Kit; For use with cobas¿ Liat Influenza A/B Assay.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2016Updated Oct 23, 2026
U.S. Cado Holdings, Inc. Recalls Imported Siluriformes Fish Products Distributed Without Meeting FSIS Requirements
High riskUsing this product could cause serious injury, illness or death — stop using it now.U.S. Cado Holdings, Inc.
USDA FSIS
Reported Jul 13, 2016
The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Ultrasonics, Inc.
FDA (openFDA device enforcement)
Reported Jul 13, 2016
HeaterBaum Foot & Ankle Heating Pad, Heating Soft Compression Therapeutic Boot with Precise Temperature Control…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ergoactives, LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
GE Healthcare, Discovery MR750w
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Image1 SPIES X-LINK Camera Control Unit (CCU), Product Model No. TC301, when used with Image1 SPIES D1 camera head,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Item # 4042-CPR Rescue Kit, containing CPR shield with one way valve & barrier filter. brand Lifeline, UPC 845174004429…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline First Aid LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Domaine de Provence La Cucina Tart Shells Produced Exclusively for Sid Wainer& Son, New Bedford, MA UPC Code:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sid Wainer And Son
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 13, 2016
Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Wegmans Fudgy & Chewy Brownies with Chocolate Chips 14 oz., UPC#7789032990
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wegmans Food Markets, Inc.
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 6, 2016
PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Bigger-Better-Bladder With 3/8" ID tubing, ITEM BBB38
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Circulatory Technology Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Dako HER2 CISH pharmDx Kit, product code: SK 109 Product Usage: For in vitro diagnostic use. HER2 CISH pharmDx Kit is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dako North America Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dynarex Corporation
FDA (openFDA device enforcement)
Reported Jul 6, 2016
MOSAIQ Oncology Information System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jul 6, 2016
K-wire, Smooth Double-pointed 0.8 x 90mm, a component of the METASURG Capture Screw System The K-wire is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nephron Pharmaceuticals Corp.
1 more product 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.