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. 2,863 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
2,863 in last 12 months

Showing 76617680 of 13,473 recalls

DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Pediatric IV Kit. Packaged in USA for Medline Industries Recalled by...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Aplicare Povidone-Iodine Prep Pad Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Concordia Trunk Kit. Packaged for Medline Industries Recalled by...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Incision and Drainage Tray Kit Recalled by Medline Industries Inc...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Newborn Kit. Packaged for Medline Industries Recalled by Medline...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Central Line Dressing Change Tray Kit Recalled by Medline Industries...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline General Purpose Instrument Set Recalled by Medline Industries Inc...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Abdominal Surgery II Pack-LF Recalled by Medline Industries Inc Due...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Skin Stapler RMVR Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Gel USP Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Cross contamination with other products: traces of Dapsone were found in the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: RHINO 7 Platinum 5000 Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Baxter Healthcare Corporation

Recalled Item: Intralipid 20% Recalled by Baxter Healthcare Corporation Due to Temperature...

The Issue: Temperature Abuse: A portion of this product lot was exposed to subfreezing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: grande X 5800 capsule Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Becton Dickinson & Company

Recalled Item: ChloraPrep OneStep (Clear) (2% w/v chlorhexidine gluconate (CHG) and 70%...

The Issue: Labeling; Label Mixup; the immediate package is labeled incorrectly as...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: PapaZen 3300 capsule Recalled by Gadget Island, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 15, 2017· Gadget Island, Inc

Recalled Item: FIFTY SHADES 6000 capsule Recalled by Gadget Island, Inc Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 14, 2017· Medisca, Inc.

Recalled Item: Aminocaproic Acid Recalled by Medisca, Inc. Due to CGMP Deviations: Product...

The Issue: CGMP Deviations: Product manufactured for Industrial Use but was labeled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2017· Vi-Jon, Inc.

Recalled Item: Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 Recalled by...

The Issue: Failed Stability Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund