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. 1,041 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 28061–28080 of 55,602 recalls
Recalled Item: Quasar MD Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution Recalled by...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is Recalled...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is...
The Issue: Atellica Solution system software (SW) version 1.13 and lower, five (5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 Recalled by...
The Issue: An incorrect control board and firmware installed in some of the Hand Held...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage:...
The Issue: QFix has advised Mevion Medical Systems that they are identifying...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3D TOP Ceiling Stand Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: In rare cases of insufficient maintenance or high clinical workload, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Quasar Plus Recalled by Quasar Bio-Tech, Inc. Due to Quasar did not...
The Issue: Quasar did not receive FDA clearance for claims of collagen/elastin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neostigmine Methylsulfate Injection Solution Recalled by Fagron Compounding...
The Issue: Labeling: Label Error on Declared Strength: syringes of Neostigmine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neostigmine Methylsulfate Injection Solution Recalled by Fagron Compounding...
The Issue: Labeling: Label Error on Declared Strength: syringes of Neostigmine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sisel Recalled by Sisel International Llc Due to Firm is recalling SiselRipt...
The Issue: Firm is recalling SiselRipt due to the presence of an unapproved artificial...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal...
The Issue: The recalled dietary supplement has the potential to contain undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system Recalled by...
The Issue: If the beam model has a highly asymmetric primary source, it is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Infinity XR2 Base Unit-Extended Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT Recalled by Integra LifeSciences...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD INFINITY XR2 BASE UNIT Recalled by Integra LifeSciences Corp. Due...
The Issue: There is a potential for the knob assembly in the swivel adapter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Neonatal Flow Sensor Cable used on devices CARESCAPE R860 Recalled by...
The Issue: The Neonatal Flow Sensor Cable may be missing the connector housing exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daptomycin for Injection Recalled by PFIZER Due to Microbial Contamination...
The Issue: Microbial Contamination of Sterile Products: Product associated with reports...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Oral Suspension USP Recalled by LUPIN SOMERSET Due to...
The Issue: Subpotent Drug and Failed Content Uniformity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.