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. 1,042 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 26861–26880 of 55,602 recalls
Recalled Item: Alprostadil 500 mcg/mL Injectable Recalled by Westlab Pharmacy, Inc. dba...
The Issue: Incorrect Product Formulation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADAA Cataract Drops Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclosporine 1% Human Eye Drops Recalled by Westlab Pharmacy, Inc. dba...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets...
The Issue: Defective Container: Customer complaints of punctures in the bottle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 Recalled by...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu Aura40 Standard Recalled by Besmed Health Business Corporation Due to...
The Issue: Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MORTON NATURAL SEA SALT ALL PURPOSE***NET WET 26 OZ (1 Recalled by MORTON...
The Issue: Iodized sea salt was packaged in Morton Natural Sea Salt packages.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Ophthalmic Solution 0.05% Recalled by Akorn, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications:out-of-specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 460 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan LeadCare¿ II Blood Lead Test Kit. In Vitro Test Recalled by...
The Issue: Defect with the calibration button for lot 1808M. Level 1 and Level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 11 mm x 340 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 130 11 mm x 340 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 400 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.