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. 968 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
968 in last 12 months

Showing 44401–44420 of 55,602 recalls

Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUX Material Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
FoodDecember 3, 2014· Giant Eagle, Inc.

Recalled Item: Jumbo Lump Crab Cakes packed from bulk into clam shell Recalled by Giant...

The Issue: Ingredient statement failed to declare milk

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 3, 2014· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2014· Hospira Inc.

Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...

The Issue: Failed Stability Specifications: Product is subpotent and has out of...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2014· House Of Flavors, Inc.

Recalled Item: Dark Cocoa Sorbetto packed in 14 oz. plastic jars Recalled by House Of...

The Issue: Undeclared milk was found in 14 oz. Dark Cocoa Sorbetto gelato manufactured...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2014· ReNew Life Formulas, Inc.

Recalled Item: PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle Recalled by...

The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2014· ReNew Life Formulas, Inc.

Recalled Item: PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs...

The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerator: ARTISTE Recalled by Siemens Medical Solutions...

The Issue: Use of any unauthorized third-party components on Siemens LINACs may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2014· Stelkast Co

Recalled Item: EXp Tibial Insert Recalled by Stelkast Co Due to Difficulty locking EXp...

The Issue: Difficulty locking EXp tibial inserts into tibial trays, caused by a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife Dual- Recalled by Vyaire Medical Due to Manufacturing error...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number:...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife single-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult AirLife dual-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
FoodNovember 27, 2014· Golden Chocolate International, Inc.

Recalled Item: Golden Chocolate ROGALIK PAPAYA Recalled by Golden Chocolate International,...

The Issue: Golden Chocolate International, Inc. has recalled (3) products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodNovember 27, 2014· Golden Chocolate International, Inc.

Recalled Item: Golden Chocolate OREX Recalled by Golden Chocolate International, Inc. Due...

The Issue: Golden Chocolate International, Inc. has recalled (3) products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodNovember 27, 2014· Golden Chocolate International, Inc.

Recalled Item: Golden Chocolate RAISIN POUND CAKE Recalled by Golden Chocolate...

The Issue: Golden Chocolate International, Inc. has recalled (3) products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund