Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,831 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,831 in last 12 months

Showing 59415960 of 29,505 recalls

Medical DeviceJuly 6, 2023· Aquila Corporation

Recalled Item: APK2 Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation Due...

The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2023· Aquila Corporation

Recalled Item: SofTech Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation...

The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Total Hip Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The prep solution included in the Total Hip Kit expires prior to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2023· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...

The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2023· Philips Ultrasound, Inc.

Recalled Item: 3D9-3v Transducer Recalled by Philips Ultrasound, Inc. Due to Transducer, an...

The Issue: Transducer, an ultrasound system accessory, consists of two parts that are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2023· Cardiac Assist, Inc

Recalled Item: LifeSPARC Pump (part number 5800-0000) contained within TandemLife LifeSPARC...

The Issue: Epoxy used during manufacturing of the LifeSPARC Pump may have uncured...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Wireless Foot Switch distributed with Philips Allura Xper and Azurion...

The Issue: Loss of availability of the wireless foot switch during procedures.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2023· Abiomed, Inc.

Recalled Item: Impella RP Flex with SmartAssist intracardiac microaxial blood pump Recalled...

The Issue: A higher than expected rate of thrombus formation or deposition has been...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 28, 2023· Stryker Corporation

Recalled Item: stryker 3.0MM Neuro Match Head Recalled by Stryker Corporation Due to There...

The Issue: There is potential the device inside the package may not match the product...

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

Class II — Potential Health HazardOngoing