Product Recalls in Indiana
Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,741 recalls have been distributed to Indiana in the last 12 months.
Showing 5901–5920 of 29,228 recalls
Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 2 Readers Recalled by Abbott Diabetes Care, Inc. Due to If...
The Issue: If blood glucose monitoring system users attempt to start a new sensor, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD HORIZON Spinal System Solera Awl Tip Tap Recalled by Medtronic Sofamor...
The Issue: Incorrect Laser Marking - Solera Awl Tip Tap
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Gamma-Glutamyl Transferase-IIn vitro diagnostic use in the...
The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica¿ CH HDL Cholesterol- In vitro diagnostic use in the Recalled by...
The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Total Bilirubin_2 -In vitro diagnostic use in the Recalled by...
The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCount+ Software Application-indicated as an adjunctive technology for...
The Issue: Potential for current software to miscount when scanning in multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH LDL Cholesterol- In vitro diagnostic use in the Recalled by...
The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Five S 5 3x65 Recalled by Karl Storz Endoscopy Due to Flexible intubation...
The Issue: Flexible intubation endoscopes sterility assurance can not be confirmed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIF AMP Recalled by Alphatec Spine, Inc. Due to Awl instrument adjustable...
The Issue: Awl instrument adjustable drill button assembly assembled in the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.