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. 1,829 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 42761–42780 of 55,602 recalls
Recalled Item: Vilex Recalled by Vilex In Tennessee Inc Due to Incidence of breakage is...
The Issue: Incidence of breakage is higher than expected.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vilex Recalled by Vilex In Tennessee Inc Due to Incidence of breakage is...
The Issue: Incidence of breakage is higher than expected.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere i Influenza A & B Product Usage: The Alere i Influenza A and B assay...
The Issue: High invalid rate and an increased risk of false negative results with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NITROFURANTOIN MONOHYDRATE/MACROCRYSTALS CAPSULES Recalled by Alvogen, Inc...
The Issue: Failed Dissolution Specification; 6 month time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EXPEDIUM Spine System/Synapse System Recalled by DePuy Spine, Inc. Due to...
The Issue: Device does not mate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Modules resetting. This failure mode happens when the Spacelabs Command...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IC-GREEN (indocyanine green for injection Recalled by Akorn, Inc. Due to...
The Issue: Subpotent Drug: Low out-of-specification potency result of the drug product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gromex Camaron Molido (Ground Shrimp) Recalled by Gromex Inc. Due to...
The Issue: Camaron Molido Ground Shrimp sampling analysis revealed the product contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Suction Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glaucoma Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knee Arthro Pack and Knee Arthro Pack II - contains Recalled by Stradis...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lima Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mississippi Pack - contains Devon Light Glove Used during surgery Recalled...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthroscopy Pack - contains Devon Light Glove Used during surgery Recalled...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phleb Pack and Laser Phleb Pack - contains Devon Light Recalled by Stradis...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shoulder Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endovenous Kit Recalled by Stradis Healthcare, LLC. Due to Convenience kits...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasc Custom Kit - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skin and Vein Pack - contains Devon Light Glove Used during surgery Recalled...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Pack and General Surgery Pack - contains Devon Light Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.