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. 1,939 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 29321–29340 of 55,602 recalls
Recalled Item: labetalol HCl injection 20 mg/4 mL (5mg/mL) Recalled by SCA Pharmaceuticals,...
The Issue: Labeling; Incorrect or Missing Lot number/Expiration Date; some product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pink flexible Recalled by Ikea North America Srvcs Inc Due to Possible Pest...
The Issue: Possible Pest Contamination at production facility.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: cobas b 221 AutoQC Module Complete Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and Recalled...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221<6>Roche OMNI S6 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 221<4>Roche OMNI S4 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atropine Sulfate Ophthalmic 1% Solution Recalled by Akorn, Inc. Due to...
The Issue: Failed Stability Specification: OOS low viscosity results discovered during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT 2.96oz (84g)...
The Issue: Mold growth on product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g) Recalled...
The Issue: Mold growth on product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Vegan Buffalo Chicken Bites Recalled by Sunneen Health Foods,...
The Issue: The firm is recalling the products listed below because it is mislabeled....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Emerald brand Glazed Walnuts Recalled by Snyder's-Lance Inc. Due to...
The Issue: Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: True 3D Viewer Recalled by Echopixel, Inc. Due to With certain software...
The Issue: With certain software versions, import of enhanced ultrasound formatted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clariti 1 day (-1.25) 90 pack Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 125II Assay Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Upon dilution, some patient samples may exhibit over-recovery outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 56% 1 Day Silicone Hydrogel (-4.50) Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clariti 1 day/Fresh Day 90 pack (-1.00) Recalled by CooperVision Inc. Due to...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 56% 1 Day Silicone Hydrogel (-2.50) Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 with 4.1.7 XX026 software version model number 728231 Recalled...
The Issue: Surview scan with tube current lower than 30 mA is unable to be initialized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.