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. 1,978 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,978 in last 12 months

Showing 2678126800 of 55,602 recalls

Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp Recalled...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Smiths Medical ASD Inc.

Recalled Item: Jelco(R) ViaValve(TM) safety intravenous (I.V.) catheters Recalled by Smiths...

The Issue: Several lots of Jelco¿ ViaValve" safety intravenous (I.V.) catheters...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Microfixation RapidFlap System 20MM RapidFlap SpinDown Clamp :...

The Issue: Spin Down RapidFlap nut that interfaces with the outer plate was assembled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· Coltene Whaledent Inc

Recalled Item: ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Recalled by...

The Issue: ParaPost Plus Titanium Posts contain stainless steel post that are a size 4

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to The...

The Issue: The catheter failed the endotoxin testing.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2018· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: These catheters may have the following deficiencies: 1) barium sulfate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Calcium Gluconate injectable Recalled by Auro Pharmacies, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Methyl-Cobalamin injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Folic Acid injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: CoEnzyme-Q10 injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Testosterone Enanthate/Cypionate injectable Recalled by Auro Pharmacies,...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Testosterone Cypionate/Enanthate injectable Recalled by Auro Pharmacies,...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Dexpanthenol injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Auro Pharmacies, Inc.

Recalled Item: Methyl-Cobalamin injectable Recalled by Auro Pharmacies, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Inadequate processes and equipment to assure...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2018· Mayne Pharma Inc

Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Mayne Pharma Inc Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is...

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

Class III — Low RiskOngoing
Refund