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. 2,752 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,752 in last 12 months

Showing 35013520 of 13,412 recalls

DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Vancomycin HCl Recalled by Edge Pharma, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Lidocaine HCL / Bupivacaine HCL (contains Hyaluronidase 15 units/mL)...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: PHENYLephrine Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Trypan Blue 0.03% Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: LT Topical Cream Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Vancomycin HCl in 0.9 % Sodium Chloride Injection Recalled by Edge Pharma,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Ceftazidime Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: CSF Otic Insufflation Capsule Recalled by Edge Pharma, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Methotrexate Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Tetracaine HCl Nasal Solution Recalled by Edge Pharma, LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenylephrine HCl Recalled by Edge Pharma, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Physicians CARE Extra Strength PAIN RELIEVER [Acetaminophen Recalled by...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Extra Strength Headache (acetaminophen 250 mg Recalled by Medique Products...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Medique Products

Recalled Item: Medique Pain-Off (Acetaminophen 250 mg Recalled by Medique Products Due to...

The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Valisa MFG LLC

Recalled Item: kleantouch HAND SANITIZER (ethyl alcohol 70%) Recalled by Valisa MFG LLC Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx7 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree sample boxes Recalled by Dental Alliance Holdings LLC Due to...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Gilead Sciences, Inc.

Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: investigation into a customer complaint...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

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

Class III — Low RiskOngoing
Refund