Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,451 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,451 in last 12 months

Showing 2638126400 of 28,355 recalls

Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 10mm X 32cm Regular Tip Recalled by Stryker...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 32cm Regular Tip Recalled by Stryker...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 2mm X 34cm Regular Tip with No Hole...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: 5mm X 32cm Regular Tip with No Holes...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2013· Stryker Endoscopy

Recalled Item: Stryker Irrigator Reusable Tips: Vented Tip Recalled by Stryker Endoscopy...

The Issue: The pre-vacuum steam sterilization (wrapped method) temperature in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· GE Healthcare, LLC

Recalled Item: GE PET Discovery 610 Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: A) Presource PBDS Recalled by Cardinal Health, Medical Products & Services...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand RPM Respiratory Gating System Recalled by Varian Medical...

The Issue: Varian has identified an anomaly with the RPM Respiratory Gating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Cardinal Health, Medical Products & Services

Recalled Item: Presource PBDS Recalled by Cardinal Health, Medical Products & Services Due...

The Issue: Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Crimpers Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Holes in the sterile barrier pouch may be caused by handling of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2013· Owens & Minor Distribution, Inc.

Recalled Item: MediChoice¿ Rayon Tipped OB/GYN Applicator Recalled by Owens & Minor...

The Issue: Owens & Minor Distribution, Inc. is conducting a market withdrawal of...

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

Class II — Potential Health HazardOngoing