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. 1,129 recalls have been distributed to Indiana in the last 12 months.
Showing 7581–7600 of 29,228 recalls
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte Liquid Acid concentrate Recalled by Fresenius Medical Care...
The Issue: The "Nominal Chemical Composition" section of the label incorrectly lists...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 340334) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...
The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...
The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995)...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB EYE MUSCLE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is an incorrect manufacturing date/timestamp within the software which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to There is an...
The Issue: There is an incorrect manufacturing date/timestamp within the software which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INBONE Tibial Tray Recalled by Wright Medical Technology, Inc. Due...
The Issue: The tibial tray lock detail is oversized (larger than specification).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE CVC BARRIER KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an orthopedic blade Recalled...
The Issue: Incorrect configuration of the blades in the package. The blades curve to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE RADIOLOGY PROCEDURE PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB BASIC OPHTHALMIC PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INBONE Tibial Tray Recalled by Wright Medical Technology, Inc. Due...
The Issue: The tibial tray lock detail is oversized (larger than specification).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB CATARACT TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE LITHOTOMY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB PHACO PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB EYE PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.