Product Recalls in Pennsylvania
Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,878 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 5501–5520 of 55,602 recalls
Recalled Item: Luminos dRF Max- Intended to visualize anatomical structures by converting...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multitom Rax -Intended to visualize anatomical structures by converting an...
The Issue: The support arm may unintentionally lower resulting in injury to persons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis Recalled by...
The Issue: Affected product has an increased risk of postoperative perisprosthetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leona's Ice Cream Recalled by Leona's Due to The product has cross...
The Issue: The product has cross contamination with peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...
The Issue: Due to packaging defects, sterility assurance and heparin activity may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling
The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...
The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: . PLT010. Indigenous Collection Signature Plates set - Dancing Recalled by...
The Issue: Glazed ceramic plates are recalled because they may exceed FDA guidance...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Code 772665860083 Recalled by Canadian Art Prints Due to Glazed ceramic...
The Issue: Glazed ceramic plates are recalled because they may exceed FDA guidance...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fludrocortisone Acetate Tablets Recalled by Teva Pharmaceuticals USA, Inc...
The Issue: Failed Impurities/Degradation Specifications: Product is being recalled due...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Failed Dissolution Specifications: results below specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PST 500 U Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX450 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX550 with L.x and M.x Recalled by Philips North...
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premo King Club Footlong 11.5oz Recalled by Lipari Foods Operating Company,...
The Issue: Potential contamination with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.