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. 2,560 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,560 in last 12 months

Showing 2400124020 of 53,528 recalls

DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Cleocin Phosphate Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Cleocin Phosphate (clindamycin injection) Recalled by Pfizer Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Cleocin Phosphate Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Estee Lauder Inc

Recalled Item: Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15 Recalled...

The Issue: Defective container: Ineffective seal between the cap and jar of the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2019· Response Biomedical Corp.

Recalled Item: Randox Laboratories Ltd. Catalogue Number CQ5052 Recalled by Response...

The Issue: The form received three complaints related to the user obtaining a result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC RP & Tri Ch Hex WP Recalled by Nobel Biocare...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Guided Start Drills/Counterbore NobRpl NP - Product Usage: The Guided...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered 6.0 6x8 mm Single-Pat - Product Usage: Drills Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Dense Bone Drill NP 3.5x16 mm Single-Pat - Product Usage: Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered WP 5x11.5 mm Single-Pat - Product Usage: Drills Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Trilliant Surgical, LLC

Recalled Item: Gridlock Ankle Screw Driver Bit - Product Usage: Recalled by Trilliant...

The Issue: A screwdriver used to facilitate implant insertion and removal was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC NP & Ext Hex WP 22 Recalled by Nobel Biocare...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered NP 3.5x11.5 mm Single-Pat - Product Usage: The Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC 3.0 31 mm- Product Usage: They Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument Hex & Tri-Ch NP/RP 22mm - Product Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered RP 4.3x10 mm Single-Pat - Product Usage: The Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered RP 4.3x11.5 mm Single-Pat - Product Usage: The Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Dense Bone Drill WP 5x13 mm Single-Pat - Product Usage: Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing