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. 2,890 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 3541–3560 of 13,473 recalls
Recalled Item: Extra Strength Headache (acetaminophen 250 mg Recalled by Medique Products...
The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medique Pain-Off (Acetaminophen 250 mg Recalled by Medique Products Due to...
The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx7 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx21 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 Recalled by Dental...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CariFree sample boxes Recalled by Dental Alliance Holdings LLC Due to...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: investigation into a customer complaint...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telmisartan and Hydrochlorothiazide Tablets Recalled by Torrent Pharma Inc....
The Issue: Superpotent; Hydrochlorothiazide
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Recalled by Teligent Pharma, Inc. Due to Superpotent...
The Issue: Superpotent Drug: Minimally superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Pfizer Inc. Due to Lack of sterility...
The Issue: Lack of sterility assurance: bag has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Recalled by Teligent Pharma, Inc. Due to Superpotent...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moxifloxacin Recalled by Denver Solutions, LLC DBA Leiters Health Due to...
The Issue: Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Old Spice Recalled by The Procter & Gamble Company Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Old Spice Recalled by The Procter & Gamble Company Due to CGMP Deviation;...
The Issue: CGMP Deviation; manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.