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. 1,184 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 621–640 of 29,947 recalls
Recalled Item: Pollen Allergy Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illegally Marketed Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neurotransmitters Plus Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adrenal Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parasite Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candida Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iodine Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intestinal Worms Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MPOX Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Downstream Occlusion alarms may occur during procedures using low flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcohol (ALC) Test Saliva Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gonorrhea test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ovulation Test (5 tests) Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitamin D-Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorbitol Intolerance Test Recalled by GET TESTED INTERNATIONAL AB Due to...
The Issue: Distribution without premarket approval/clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software...
The Issue: A software timing and processor communication issue in MiniMed" 780G...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OER-Elite Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...
The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX700. Product Number: 865241. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500. Product Number: 866064. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400. Product Number: 866060. Recalled by...
The Issue: Potential issue where the IntelliVue monitors did not alarm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.