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. 2,140 recalls have been distributed to Indiana in the last 12 months.
Showing 6441–6460 of 53,528 recalls
Recalled Item: The GOAT SUBLINGUAL STRIP Recalled by Pyramids Wholesale Inc. Due to...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SILVERBACK XXX POWER MALE ENHANCEMENT Recalled by Pyramids Wholesale Inc....
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Weiner Boner Honey Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ALPHASTRIP MALE PERFORMANCE ENHANCER Recalled by Pyramids Wholesale Inc. Due...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: libigrow RED DRAGON+ Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GoHARD 25000 Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Allia IGS 7 Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 5 Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Interact Discovery RT Recalled by GE Medical Systems, SCS Due...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 6 Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightStrike Blackout Curtains Recalled by XENEX Disinfection Services Inc....
The Issue: Blackout curtains are no longer recommended as a protective barrier against...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 7 OR Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERLA TL 25D SCREW 45 25-S TLF-DS 45 Recalled by SPINEART SA Due to Due to...
The Issue: Due to receiving information regarding difficulties with the insertion of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Seprafilm Adhesion Barrier 1 Half Sheet Recalled by Baxter Healthcare...
The Issue: Product was distributed in the United States without proper regulatory approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm)...
The Issue: Products may not be heparin coated as indicated on the label-leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga...
The Issue: Due to complaints of particulates, residue, occlusions, and bent tips for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x Recalled by...
The Issue: Products may not be heparin coated as indicated on the label-leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: a. Medline CC Drawer 4 IV Circulation Recalled...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.