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. 1,086 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 16701–16720 of 55,602 recalls
Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 70 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 45 Recalled by...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 100+ Recalled...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One...
The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLASH Ostial System Recalled by Ostial Corporation Due to Angioplasty system...
The Issue: Angioplasty system has a manufacturing issue that has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models:...
The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew BHR SQUARE HEADED NAIL Recalled by Smith & Nephew Orthopaedics...
The Issue: The nail head may become detached during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pipeline Flex Embolization Device Recalled by Micro Therapeutics Inc, Due to...
The Issue: Due to potential push wire fractures in the delivery system during use. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 Pipeline Flex Embolization Device with Flex Shield Technology Recalled...
The Issue: Due to potential push wire fractures in the delivery system during use. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: Due to intermittent failures of the power supply in the ultrasound system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System . An automated immunoassay analyzer for Recalled by Abbott...
The Issue: A design defect (hardware and software) allows liquid waste pressure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beta-Hydroxybutyrate Reagent A - Enzyme (unlabeled). in vitro diagnostic...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron CX/DX/LX Beta-Hydroxybutyrate . in vitro diagnostic reagent....
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Beta-Hydroxybutyrate . in vitro diagnostic reagent. Recalled...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent. Recalled by...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Beta-Hydroxybutyrate LiquiColor for Synchron CX/LX/DX. in...
The Issue: Deterioration in the stability of the reagents which has resulted in lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Molding & Occlusion Balloon Catheter Recalled by W. L. Gore &...
The Issue: Complaints received concerning Balloon Catheter leakage from the guidewire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.