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. 2,696 recalls have been distributed to Indiana in the last 12 months.
Showing 13321–13340 of 29,228 recalls
Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...
The Issue: The instrument holder may be sent on a trajectory that is not within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Users may experience intermittent slide dispense issues with some cartridges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...
The Issue: The canister neck bushing may become loose and separate from the body of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...
The Issue: The canister neck bushing may become loose and separate from the body of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canister HFC-134a / 980g Recalled by Candela Corporation Due to The canister...
The Issue: The canister neck bushing may become loose and separate from the body of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...
The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canister HFC-134a /980g Recalled by Candela Corporation Due to The canister...
The Issue: The canister neck bushing may become loose and separate from the body of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...
The Issue: The recall is being conducted due to a potential defective component on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...
The Issue: The touchpad may not work properly after cleaning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: Instruments were manufactured with a shortened 30mL reagent draw straw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron Systems Opiate 2000 ng Reagent (OP2 1 x 250) Recalled by Beckman...
The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opiate 300 Ng Reagent (OP 1 X 250) for use Recalled by Beckman Coulter Inc....
The Issue: Cross-reactivity testing may not meet the claims indicated in the Opiate 300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...
The Issue: It is possible that the forced electron density settings will be changed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Express Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achilles Insight Bone Sonometer Recalled by GE Healthcare, LLC Due to...
The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...
The Issue: The firm received reports of loss of audio alarm after a power failure or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.