DrugSep 23, 2020
RLC Labs WP Thyroid, Westhroid Pure, 1.75 Grain (113.75 mg) Thyroid USP recall — FDA D-1612-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
10,685drug recall records
953FDA Class I records
8firms with 5+ records
Aidapak Services, LLC537 records
Database records
Records — page 135
10,685 detailed records are currently available in this category.
DrugSep 23, 2020
RLC Labs Nature Throid, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg recall — FDA D-1615-2020
Subpotent Drug: FDA analysis found product to be subpotent
Class IFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature-Throid, Thyroid USP [liothyronine (T3) 18 mcg and levothyroxine (T4) 76 recall — FDA D-1602-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs WP Thyroid, Westhroid Pure, 1.5 Grain (97.5 mg) Thyroid USP recall — FDA D-1611-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature Throid, 2 Grain (130 mg) Thyroid USP [Liothyronine (T3) 18 mcg recall — FDA D-1618-2020
Subpotent Drug: FDA analysis found product to be subpotent
Class IFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature Throid, 3/4 Grain (48.75 mg) Thyroid USP [Liothyronine (T3) 6.75 mcg recall — FDA D-1616-2020
Subpotent Drug: FDA analysis found product to be subpotent
Class IFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
Real Clean Distribuciones SA de CV scent theory KEEP IT CLEAN, pure clean recall — FDA D-1579-2020
CGMP Deviations: Other products were recalled because they were manufactured in the same facility as the product found to contain methanol.
Class IIFDA: TerminatedReal Clean Distribuciones SA de CV
DrugSep 16, 2020
Cephalexin for Oral Suspension, USP 250 mg per 5 mL, For Reconstitution, For Oral Use Only recall — FDA D-0013-2021
CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugSep 16, 2020
Cephalexin for Oral Suspension, USP 125 mg per 5 mL, For Reconstitution, For Oral Use Only recall — FDA D-0012-2021
CGMP deviations; there is a possibility that some bottles in these lots may have the active ingredient above and/or below specification limits.
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugSep 16, 2020
Open Book Extracts Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ (1.2 mL) recall — FDA D-1563-2020
Labeling Not Elsewhere Classified: Product labeled to contain methanol
Class IIFDA: TerminatedOpen Book Extracts
DrugSep 16, 2020
Cephalexin for Oral Suspension, USP 250 mg per 5 mL, For Reconstitution, For Oral Use Only recall — FDA D-1566-2020
Sub-Potent Drug: Out of specification test results for potency (below specification).
Class IIFDA: TerminatedTeva Pharmaceuticals USA
DrugSep 16, 2020
Maquiladora Miniara Sa De Cv Shine & Clean Hand Sanitizer gel, (Ethyl Alcohol 70%), 33.81 fl recall — FDA D-1565-2020
CGMP Deviations: Products manufactured at the same site were FDA testing found below the label claim for ethanol content and the presence of undeclared methanol.
Class IIFDA: TerminatedMaquiladora Miniara Sa De Cv
DrugSep 9, 2020
SG24 Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Towelette recall — FDA D-1574-2020
Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug
Class IFDA: TerminatedSG24 LLC
DrugSep 9, 2020
Laboratorios Jaloma S.A. de C.V Jaloma Antiseptic Hand Sanitizer, Ethyl Alcohol 62% with recall — FDA D-1555-2020
cGMP deviations
Class IIFDA: TerminatedLaboratorios Jaloma S.A. de C.V.
DrugSep 9, 2020
AAA Cosmetica, SA de CV bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 recall — FDA D-1570-2020
Chemical Contamination: Product contains methanol.
Class IFDA: TerminatedAAA Cosmetica, SA de CV
DrugSep 9, 2020
Tranexamic Acid Injection, USP, 1000 mg/10 mL (100 mg/mL), 10 mL Single-Dose Vial recall — FDA D-1576-2020
Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid Injection, USP to contain vials of Amiodarone HCl Injection, USP and cartons labeled as Amiodarone HCl Injection,…
Class IFDA: TerminatedMylan Institutional LLC
DrugSep 9, 2020
Amiodarone Hydrochloride Injection, USP, 450 mg/9 mL (50 mg/mL), 9 mL Single-Dose Vial recall — FDA D-1575-2020
Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid Injection, USP to contain vials of Amiodarone HCl Injection, USP and cartons labeled as Amiodarone HCl Injection,…
Class IFDA: TerminatedMylan Institutional LLC
DrugSep 9, 2020
ROQUE PLAST, S.A. DE C.V Command Brands GelAnti Bac Instant Hand Sanitizer, 70% Alcohol, , 8 recall — FDA D-1559-2020
CGMP Deviation: Potential contamination with undeclared methanol.
Class IIFDA: TerminatedROQUE PLAST, S.A. DE C.V.
DrugSep 9, 2020
AAA Cosmetica, SA de CV bio aaa Advance Hand Sanitizer Ethyl Alcohol 70%, Unscented, 16.23 recall — FDA D-1569-2020
CGMP Deviations
Class IIFDA: TerminatedAAA Cosmetica, SA de CV
DrugSep 2, 2020
SCA Pharmaceuticals Heparin Sodium 10,000 units in 0.9% Sodium Chloride 1000 mL, Single Dose recall — FDA D-1553-2020
Cross Contamination with Other Product(s): containers labeled as having methylparaben and propylparaben as preservatives, actually contained undeclared benzyl alcohol and did not contain…
Class IFDA: TerminatedSCA Pharmaceuticals
DrugSep 2, 2020
Fresenius Kabi USA Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL recall — FDA D-1537-2020
Cross Contamination with other products: trace amounts of lidocaine
Class IFDA: TerminatedFresenius Kabi USA, LLC
DrugSep 2, 2020
Yusef Manufacturing Laboratories Rocky Mountain Sunscreen SPF30 Kiwi Flavored Lip Balm recall — FDA D-1540-2020
Superpotent Drug: Active Ingredient Octisalate found at 15% above label claim.
Class IIFDA: TerminatedYusef Manufacturing Laboratories, LLC
DrugSep 2, 2020
SCA Pharmaceuticals Heparin Sodium 2,500 units in 0.9% Sodium Chloride 500 mL, Single Dose recall — FDA D-1550-2020
Cross Contamination with Other Product(s): containers labeled as having methylparaben and propylparaben as preservatives, actually contained undeclared benzyl alcohol and did not contain…
Class IFDA: TerminatedSCA Pharmaceuticals
DrugSep 2, 2020
SCA Pharmaceuticals Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL, Single Dose recall — FDA D-1552-2020
Cross Contamination with Other Product(s): containers labeled as having methylparaben and propylparaben as preservatives, actually contained undeclared benzyl alcohol and did not contain…
Class IFDA: TerminatedSCA Pharmaceuticals
How to use this drug recall index
A drug recall record can include the reason for recall, firm, status, distribution pattern, quantity and FDA classification. This site does not provide medical advice; it organizes public recall information and links users back to official sources.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
What the database can and cannot tell you
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.