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. 2,906 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 3121–3140 of 55,602 recalls
Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis Thromboplastin-D Recalled by Fisher Diagnostics Due to...
The Issue: The incorrect value of the International Sensitivity Index (ISI) is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis Thromboplastin-D Recalled by Fisher Diagnostics Due to...
The Issue: The incorrect value of the International Sensitivity Index (ISI) is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Golden Crop Candy (10 oz. (283g) wrapped candies) Recalled by Blooming...
The Issue: Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Golden Crop Candy (8 oz. (227g) un-wrapped candies) Recalled by Blooming...
The Issue: Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...
The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne...
The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...
The Issue: Chemical Contamination: This recall has been initiated due to detected trace...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRASUGREL TABLETS Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...
The Issue: Presence of foreign substance: Presence of Benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...
The Issue: Presence of foreign substance: Presence of Benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Rising Pharma Holding, Inc....
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Coracoid Clamp Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Glenoid Digitizer Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Depth Stop Pin Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Instrument Kit Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Box Base Recalled by Tornier S.A.S. Due to...
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.