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. 1,818 recalls have been distributed to Pennsylvania in the last 12 months.

55,602 total recalls
1,818 in last 12 months

Showing 5198152000 of 55,602 recalls

Medical DeviceMarch 20, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...

The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...

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

Class II — Potential Health HazardOngoing
FoodMarch 20, 2013· Red Mill Farms

Recalled Item: individual 2 oz chocolate macaroons packaged in plastic wrapper labeled...

The Issue: A recall was initiated as a result of an undeclared sugar ingredient in the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 19, 2013· Accuray Incorporated

Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...

The Issue: A defect on the master-side connector block of the pneumatic tool changer...

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

Class II — Potential Health HazardOngoing
DrugMarch 19, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Disulfiram Tablets USP 250 mg Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: CGMP Deviation; cotton coil is missing in some packaged bottles

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

Class III — Low RiskOngoing
Refund
DrugMarch 19, 2013· Dr. Reddy'S Laboratories

Recalled Item: Tizanidine Tablets USP Recalled by Dr. Reddy'S Laboratories Due to Labeling...

The Issue: Labeling Illegible: There is a possibility that the bottle labels do not...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 19, 2013· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...

The Issue: Some patients are obtaining access to the dosage reset codes required to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...

The Issue: Some patients are obtaining access to the dosage reset codes required to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...

The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...

The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...

The Issue: Devices were not sealed correctly during the manufacturing process, and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Integra Burlington MA, Inc.

Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....

The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling

The Issue: Product may be mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: HD Still Capture System ConMed Linvatec . Captures Recalled by Linvatec...

The Issue: The VP1600 HD Still Capture Image System is recalled due to an anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Shimadzu Medical Systems

Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...

The Issue: The recall was initiated because Shimadzu Corporation has identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...

The Issue: Devices were not sealed correctly during the manufacturing process, and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: PSS Select medical products***Biopsy Punches*** Disposable manual instrument...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing