PFIZER INC recalls
Every recall we track for PFIZER INC — 123 in all, from 2012–2025 — plus the complaints and injury reports the public filed about them. 20 are rated “stop using now”.
Recalls per year, by danger level
Recalls from PFIZER INC more than doubled in 2025 (5, up from 2 in 2024). 22% rated “stop using now”.
All FDA recall records for PFIZER INC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 2 | 1 | 2 | 7 | 12 |
| 2018 | 2 | 2 | 4 | 3 | 11 |
| 2019 | 3 | 4 | 6 | 3 | 16 |
| 2020 | 3 | 1 | 2 | 1 | 7 |
| 2021 | 1 | 0 | 4 | 6 | 11 |
| 2022 | 3 | 0 | 7 | 6 | 16 |
| 2023 | 3 | 3 | 1 | 0 | 7 |
| 2024 | 1 | 0 | 0 | 1 | 2 |
| 2025 | 1 | 0 | 2 | 2 | 5 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
PFIZER INC recalls before 2017
Recalls on record by year.
Most common reasons for PFIZER INC recalls
What to do if you have a recalled PFIZER INC product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All PFIZER INC recalls
60 shown- Lower riskDrug
PFIZER INC recalls Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL
Pfizer recalls epinephrine injection vials with lot numbers LY3681, LY4360, LY4416 due to lack of sterility assurance. These vials may cause infection if used.
PfizerAug 4, 2025 - Stop using nowDrug
Pfizer Inc. recalls Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed
Pfizer recalls 1.2 million units of Bicillin L-A (penicillin G benzathine) due to particulates found during visual inspection. Affected products have specific NDC codes and expiration dates. Consumers should contact Pfizer for details.
PfizerJul 10, 2025 - Lower riskDrug
Pfizer Inc. recalls DOBUTamine Injection, USP, 250 mg/20 mL (12.5 mg/mL), 20 mL per Single-dose Vial, carton of 10 Fliptop Vials, Rx only,
Pfizer recalls 10-vial packages of DOBUTamine injection due to discoloration from cracked vials. Discarded vials may cause unsafe medication use.
PfizerMay 28, 2025 - Stop using nowDrug
Pfizer Inc. recalls Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose Carpuject, Sterile Cartridge Unit with
Pfizer recalls specific lots of Labetalol Hydrochloride Injection due to potential incomplete crimp seals and lack of sterility assurance.
PfizerMay 20, 2024 - Use cautionDrug
Pfizer Inc. recalls 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous
Pfizer recalls 4.2% sodium bicarbonate injection (5 mEq/10mL) with glass particles that could cause injury during IV use. This product was sold in specific lots and packaging.
PfizerDec 21, 2023 - Stop using nowDrug
Pfizer Inc. recalls 2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT Unit of Use Syringe, packaged as 1 vial and
Pfizer recalls 2% Lidocaine HCl Injection (100mg/5mL) with glass particulate matter. This could cause injury if injected. Affected units have specific NDC and lot numbers.
PfizerOct 2, 2023 - Lower riskDrug
Pfizer Inc. recalls MEKTOVI (binimetinib) tablets, 15 mg, 180-count bottle, Rx only, Distributed by: Array BioPharma Inc., a wholly owned
Pfizer recalls 15 mg MEKTOVI tablets due to incorrect expiration date on labels. The correct expiration is February 2025, but labels show March 2026. This affects prescription medication.
PfizerMar 8, 2023 - Stop using nowDrug
Pfizer Inc. recalls Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a)
Pfizer recalls Heparin Sodium 2,000 units per 1,000 mL bags due to potential leakage. This may cause contamination. Check your product details to see if affected.
PfizerDec 29, 2022 - Stop using nowDrug
Pfizer Inc. recalls Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton,
Pfizer recalls 1.5g vancomycin injections with glass particles that could cause serious injury during injection. Affected lots from 33045BA to 1SEP2023. Stop using immediately.
PfizerDec 22, 2022 - Lower riskDrug
Pfizer Inc. recalls Aminophylline Injection, USP 250 mg/10 mL (25 mg/mL) 25x10 mL Single-dose vial, Rx only, Distributed by Hospira, Inc.
Pfizer recalls aminophylline injection vials due to a hair complaint in one vial. This medication is prescription-only and distributed by Hospira. Check your vial's lot number and NDC code for affected products.
PfizerSep 27, 2022 - UnratedDrug
Pfizer Inc. recalls PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further
Pfizer recalls PROPOFOL Injectable Emulsion (100 mL glass vials) due to particulate matter. This may cause serious complications during medical use. Affected units have specific NDC numbers and lot numbers.
PfizerAug 22, 2022 - Stop using nowDrug
Pfizer Inc. recalls Propofol Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL per glass fliptop vial (NDC 0409-4699-54)
Pfizer recalls Propofol Injectable Emulsion vials containing a beetle particulate. This could cause serious injury if injected. Affected vials have NDC 0409-4699-54 and were distributed by Hospira.
PfizerJul 13, 2022 - UnratedDrug
Pfizer Inc. recalls Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of
Pfizer recalls Accupril 10mg tablets (NDC 0071-0530-23) due to N-nitrosoquinapril levels exceeding safe limits. This may pose a health risk. Contact Pfizer for details.
PfizerApr 22, 2022 - Lower riskDrug
Pfizer Inc. recalls quinapril and hydrochlorothiazide tablets, 20 mg/25 mg*, 90 Tablets bottles, Rx Only, Distributed by: Greenstone, LLC,
Pfizer recalls 20mg/25mg quinapril and hydrochlorothiazide tablets due to potential impurities that could exceed safe levels. This is a prescription-only product distributed by Greenstone LLC.
PfizerMar 21, 2022 - Stop using nowDrug
Pfizer Inc. recalls 5% Dextrose Injection, USP, 50 mL ADD-Vantage Unit, Rx only, Distributed by Hospira, INC., Lake Forest, IL 60045 USA,
Pfizer recalls 50mL 5% Dextrose Injection units with potential leak risk. This sterile injection product may cause contamination if the bag leaks.
PfizerNov 30, 2021 - UnratedDrug
Pfizer Inc. recalls Chantix (varenicline) tablets 0.5mg, 56 Tablets, Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc. NY, NY
Pfizer recalls Chantix 0.5mg tablets due to potential N-nitroso-varenicline impurity above FDA limits. Affected lots made in Ireland with specific NDC numbers.
PfizerAug 13, 2021 - Lower riskDrug
Pfizer Inc. recalls Chantix (varenicline) tablets, 0.5mg*, 56 Tablets, Rx Only, Distributed by Pfizer Labs, Division of Pfizer Inc., NY, NY
Pfizer recalls Chantix 0.5mg tablets due to potential presence of N-nitroso-varenicline impurity above FDA safety limits. Affected lots: 00019213 (exp 31 Jan 2022) and EC6994 (exp May 31, 2023).
PfizerJun 9, 2021 - Lower riskDrug
Pfizer Inc. recalls Sterile Water for Inj., USP, 25 x 100 mL Single Dose Vials per carton, Rx only, For Drug Diluent Use Only, Distributed
Pfizer recalls sterile water vials for injection due to insect particulate matter found in one vial. This affects specific lot numbers and requires immediate action to prevent potential contamination.
PfizerMay 3, 2021 - Lower riskDrug
PFIZER, INC recalls 0.5% Bupivacaine Hydrochloride Injection, USP, 150 mg/30 mL (5 mg/mL), 30 mL Single-dose Teartop Vials (NDC
Pfizer recalls 30mL single-dose vials of 0.5% Bupivacaine Hydrochloride Injection that may contain lidocaine instead. This labeling mix-up could lead to incorrect medication use during medical procedures.
PfizerMay 3, 2021 - Stop using nowDrug
Pfizer Inc. recalls Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL) 2 mL Single-dose Fliptop Vials, Rx only, Distributed by
Pfizer recalls specific fentanyl vials due to potential sterility issues and metal seal defects. Affected vials have NDC 0409-9094-12 and specific expiration dates. Stop using immediately if you have these vials.
PfizerJul 20, 2020 - Use cautionDrug
Pfizer Inc. recalls Unasyn (ampicillin sodium/sulbacatam) for injection, 1.5 g* per vial, Rx Only, 10 vials/carton, Made in Italy
Pfizer recalls Unasyn (ampicillin/sulbacatam) injections due to particulate matter found after reconstitution. Affected items were made in Italy with specific lot numbers and expiration dates.
PfizerMay 29, 2020 - UnratedDrug
Pfizer Inc. recalls Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg, packaged in 2 blister cards containing 15 tablets each
Pfizer recalls Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg with failed dissolution specifications. Rx-only medication distributed by Wyeth in Ireland. No remedy specified in recall notice.
PfizerMay 27, 2020 - Stop using nowDrug
Pfizer Inc. recalls Elelyso (taliglucerase alfa) for injection, 200 units/vials,, Rx only, Distributed by Pfizer Labs, Division of Pfizer
Pfizer recalls Elelyso (taliglucerase alfa) injections after reports of loose metal ferrules causing potential contamination. Affected vials have specific lot numbers and expiration dates.
PfizerFeb 27, 2020 - Lower riskDrug
Pfizer Inc. recalls Caduet (amlodipine besylate/atorvastatin calcium) Tablets, 10 mg/20 mg*, 30-count bottle, Rx only, Distributed by:
Pfizer recalls Caduet 10mg/20mg tablets due to potential defective packaging that may not seal properly, risking moisture exposure. Affected products were distributed with specific lot numbers and expiration dates.
PfizerFeb 5, 2020 - Stop using nowDrug
Pfizer Inc. recalls Fentanyl Citrate Inj., USP 100 mcg Fentanyl/2 mL (50 mcg/mL), 2 mL Single-dose Vial, Each Tray contains 25 Vials,
Pfizer recalls Fentanyl vials with loose metal seals that may compromise sterility. Affected vials have specific lot numbers and expiration dates. Stop using immediately if you have these vials.
PfizerFeb 3, 2020 - Lower riskDrug
Pfizer Inc. recalls 25% Dextrose Injection, USP 2.5 grams (250 mg/mL) 10 mL Single-dose, Rx Only, Hospira, Inc., Lake Forest, IL 60045 USA,
Pfizer recalls 25% Dextrose Injection (250 mg/mL) due to incorrect or missing expiration date on labels. This affects single-dose medical products sold to hospitals. Contact Pfizer for details.
PfizerNov 27, 2019 - Use cautionDrug
Pfizer Inc. recalls 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake
Pfizer recalls 500mL Dextrose Injection bags with potential leak risk. Affected lots expire March 2020. Stop using if leaking.
PfizerOct 2, 2019 - Lower riskDrug
Pfizer Inc. recalls Zarontin (ethosuximide capsules, USP) 250 mg, 100-count bottle, Rx Onl,y Made in Netherlands Distributed by Parke-Davis
Pfizer recalls Zarontin 250mg capsules with incorrect expiry dates on labels. The label shows 09/2021 instead of 09/2020. This could lead to medication safety issues if used beyond expiration.
PfizerSep 12, 2019 - Lower riskDrug
Pfizer Inc. recalls Bacteriostatic Water for Injection, USP, 30 mL vials, Rx only, Mfd. for: Hospira, Inc., Lake Forest, IL 60045 USA. NDC
Pfizer recalls Bacteriostatic Water for Injection vials due to lack of sterility assurance. Affected vials have specific NDC numbers and lot dates. Consumers should contact Pfizer for details.
PfizerSep 6, 2019 - Stop using nowDrug
Pfizer Inc. recalls RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b)
Pfizer recalls specific lots of RELPAX (eletriptan HBr) 40 mg tablets due to microbial contamination with Burkholderia and Pseudomonas. Check your NDC and lot numbers.
PfizerAug 14, 2019 - Use cautionDrug
Pfizer Inc. recalls Milrinone Lactate Injection 200 mcg (0.2 mg)/mL* in 5% Dextrose Injection, 20 mg/100 mL, 100 mL bag, Rx Only, Hospira,
Pfizer recalls Milrinone Lactate Injection 200 mcg/mL in 5% Dextrose due to potential leakage risks. Affected lots expired by January 2020.
PfizerJul 9, 2019 - Lower riskDrug
Pfizer Inc. recalls Relpax (eletriptan HBr) 40 mg, a) 12 tablets 2 cards x six 40 mg tablets per blister pack, NDC 0049-2340-05; b) 6
Pfizer recalls Relpax 40mg tablets due to a labeling error showing 20mg instead of 40mg per tablet. This may cause incorrect dosing. Affected products have specific NDC numbers and expiration dates.
PfizerApr 29, 2019 - Use cautionDrug
Pfizer Inc. recalls 8.4% Sodium Bicarbonate Injection, USP 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL) 50 mL Single-dose fliptop vial, 25 vials
Pfizer recalls 25 vials of 8.4% Sodium Bicarbonate Injection with glass particulates. This injection may cause serious injury if used. Contact Pfizer for details.
PfizerMar 15, 2019 - UnratedDrug
Pfizer Inc. recalls Cleocin Phosphate, clindamycin injection, USP, 900 mg/ 6 mL (150 mg/mL), 6 mL vial, Rx only, Distributed by Pharmacia &
Pfizer recalls Cleocin phosphate injection due to impurities that could cause serious harm. Patients with prescription orders should check their medication details and contact Pfizer for guidance.
PfizerMar 15, 2019 - Use cautionDrug
Pfizer Inc. recalls Levoxyl (levothyroxine sodium tablets, USP) tablets 112 mcg, 100-count bottle, Rx Only,Distributed by Pfizer Inc. New
Pfizer recalls 112 mcg Levoxyl tablets due to superpotent drug risk. This may cause serious health issues if taken without medical supervision.
PfizerDec 6, 2018 - Stop using nowDrug
Pfizer Inc. recalls Magnesium Sulfate in Water for Injection (0.325 mEq Mg++/mL) 40 mg/mL, 20 g Total, 500 mL Single-Dose Container bag, Rx
Pfizer recalls 94,752 bags of Magnesium Sulfate in Water for Injection due to a mispack hazard involving Heparin. Check your lot numbers.
PfizerOct 3, 2018 - Lower riskMedical device
Pfizer Inc. recalls Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product Usage: Provides heat therapy for temporary
Pfizer recalls Thermacare HeatWraps Menstrual with UPCs 0573302002 and 0573302044 due to complaints of wraps coming apart and leaking granular material.
PfizerOct 2, 2018 - UnratedDrug
Pfizer Inc. recalls Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle, Rx only Distributed by: Greenstone LLC.
Pfizer recalls 500-tablet Glipizide XL 5mg bottles (Rx only) due to manufacturing deviations. Affected lots were used in final production. Consumers should contact Pfizer for details.
PfizerSep 20, 2018 - Stop using nowDrug
Pfizer Inc. recalls Meropenem for Injection, USA (I.V.), 1 gram/vial, 25 vials per carton, Sterile, Rx Only, Manufactured for: Hospira,
Pfizer recalls Meropenem for Injection (1g/vial) due to potential loss of container integrity, risking contamination. Affected lots manufactured for Hospira in Lake Forest, IL. Stop using immediately.
PfizerSep 20, 2018 - Use cautionDrug
Pfizer Inc. recalls Elelyso (taliglucerase alfa) for injection, 200 units/vial, single-use vial, Rx only, Distributed by Pfizer Labs,
Pfizer recalls Elelyso (taligl: 200 units/vial) injections due to loose metal ferrule crimps that may cause contamination. Affected lots include S91616. Patients should contact their doctor for guidance.
PfizerSep 19, 2018 - UnratedDrug
Pfizer Inc. recalls Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 2.5 mL Single-use Vial, Rx only, Sterile, Manufactured for: Hospira,
Pfizer recalls Argatroban injection vials due to impurities and stability issues. Patients with blood clotting conditions should contact their doctor immediately.
PfizerAug 28, 2018 - Lower riskDrug
Pfizer Inc. recalls Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation.
Pfizer recalls 10 mg/mL hydromorphone injection vials that may be empty or cracked, posing a risk of contamination. Affected vials have specific NDC and expiration dates.
PfizerFeb 7, 2018 - Lower riskDrug
Pfizer Inc. recalls Zoloft (sertraline HCl) tablets 25 mg* 30-count bottle, Rx only, Distributed by Roerig Division of Pfizer Inc., NY, NY,
Pfizer recalls Zoloft 25mg tablets due to weight variations causing subpotent or superpotent tablets. This may affect prescription medication safety. Check your NDC 0049-4960-30 lot S84026.
PfizerOct 20, 2017 - Stop using nowDrug
Pfizer Inc. recalls Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL
Pfizer recalls sterile water vials with potential cracked glass that could cause contamination. Affected vials were manufactured by Hospira in Lake Forest, IL. Stop using if you have these vials.
PfizerSep 1, 2017 - Use cautionDrug
Pfizer Inc. recalls Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA.
Pfizer recalls Vancomycin Hydrochloride 750mg sterile powder for injection due to glass particles in vials. This poses a risk of serious injury during medical use. Affected products include specific lots from Hospira.
PfizerAug 30, 2017 - Stop using nowDrug
Pfizer Inc. recalls HYDROmorphone HCl Injection, USP, 2 mg/mL, 1mL Single-use vial, packaged in cartons of 25 vials, Rx only, Hospira,
Pfizer recalls specific lots of Hydromorphone HCl Injection due to lack of sterility assurance. Check your vials for lot number 760853A.
Pfizer / HospiraAug 22, 2017 - UnratedDrug
Pfizer Inc. recalls Quillivant XR methylphenidate HCl, for extended-release oral suspension, 750mg/150 mL total volume (When constituted
Pfizer recalls Quillivant XR methylphenidate HCl oral suspension due to failed dissolution specifications. This medication may not release properly when taken, potentially affecting effectiveness. Contact Pfizer for details.
PfizerAug 4, 2017 - UnratedDrug
Pfizer Inc. recalls Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular,
Pfizer recalls Deferoxamine Mesylate injection vials due to color change impurity during manufacturing. Affected lots may pose safety risks; contact Pfizer for details.
PfizerJul 12, 2017 - Lower riskDrug
Pfizer Inc recalls Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only,
Pfizer recalls Quillivant XR (methylphenidate) oral suspension due to failed dissolution testing at 12 months. This medication is prescription-only and distributed by NextWave Pharmaceuticals.
PfizerMar 7, 2017 - Lower riskDrug
Pfizer Inc. recalls PROTONIX I.V. (pantoprazole sodium) for Injection, Equivalent to 40 mg pantoprazole per vial, For I.V. infusion only,
Pfizer recalls PROTONIX I.V. (pantoprazole sodium) for injection due to potency issues at 6-month stability. This may affect drug effectiveness. Check your vial lot numbers for recall.
PfizerNov 22, 2016 - Use cautionDrug
Pfizer Inc. recalls LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by:
Pfizer recalls LEVOXYL 200 mcg tablets (100-count) for superpotent risk. This may cause overmedication if taken without medical supervision.
PfizerNov 7, 2016 - Lower riskDrug
Pfizer Inc. recalls PREMARIN (conjugated estrogen tablets, USP) 1.25 mg, 1000- count bottle, Rx only, Distributed by: Wyeth Pharmaceuticals
Pfizer recalls PREMARIN 1.25 mg tablets due to incorrect expiry date labeling. Affected bottles may have an expiry date of 11/17 instead of 09/17. Consumers should check labels and contact Pfizer for guidance.
PfizerSep 15, 2016 - UnratedDrug
Pfizer Inc. recalls Cytotec (misoprostol) Tablets, 200 mcg, 100 Tablets blister pack (10X10), For in-institution use only, Rx only,
Pfizer recalls Cytotec misoprostol tablets due to impurities and degradation products found in some lots. These tablets are for institutional use only and require a prescription.
PfizerSep 9, 2016 - Lower riskDrug
Pfizer Inc. recalls Zoloft (sertraline HCl) tablets, 100 mg*, 30 count bottles, Rx only, Distributed by Roerig, Division of Pfizer, Inc.,
Pfizer is recalling specific lots of Zoloft (sertraline HCl) 100 mg tablets because they failed specifications for tablet thickness. Check your bottle's lot number.
PfizerApr 28, 2016 - Use cautionDrug
Pfizer Inc recalls Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid 8 oz. Bottle (237 mL), Distributed by Pfizer, Madison, NJ
Pfizer recalls Adult Robitussin PEAK COLD DM Liquid due to a label mix-up. Check your bottle's lot number and expiration date for details.
RobitussinFeb 10, 2016 - Use cautionDrug
Pfizer Inc. recalls Lyrica (pregabalin) capsules, 75 mg, 90-count bottle, Rx only, Distributed by: Parke-Davis, Division of Pfizer Inc.,
Pfizer is recalling specific lots of Lyrica (pregabalin) capsules because some may be deformed or damaged. Check your bottle's lot number and expiration date.
PfizerJan 11, 2016 - Use cautionDrug
Pfizer Inc. recalls Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC
Pfizer recalls Norpace CR extended-release capsules due to failed dissolution specifications. Check lot numbers C150064 and C150065 for expiration date 6/16.
PfizerDec 2, 2015 - Use cautionDrug
Pfizer Inc. recalls Xanax (alprazolam) tablets, 0.25 mg, 100-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co. Division of
Pfizer is recalling specific lots of Xanax (alprazolam) 0.25 mg tablets because they may be subpotent, meaning they might not contain the full amount of active ingredient.
PfizerSep 24, 2015 - Use cautionDrug
Pfizer Inc. recalls Oxecta(TM) (oxycodone HCl) tablets, 5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King
Pfizer recalls specific Oxecta 5 mg tablets due to failed impurity specifications. Check lot numbers and expiration dates for affected units.
OxectaFeb 26, 2015 - Use cautionDrug
Pfizer Inc. recalls Tikosyn (dofetilide) 125 mcg (0.125 mg), a) 14-count bottle (NDC 0069-5800-61), b) 60-count bottle (NDC 0069-5800-60),
Pfizer recalls specific lots of Tikosyn (dofetilide) 125 mcg capsules due to potential cracked or broken capsules. Check your bottle NDC and lot numbers.
PfizerDec 3, 2014
PFIZER INC recall questions
How many recalls has PFIZER INC had?
123 recalls from PFIZER INC are on record with U.S. safety agencies, from 2012–2025 (120 drug, 3 medical device).
What is the most recent PFIZER INC recall?
PFIZER INC recalls Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL, dated Aug 4, 2025. Every PFIZER INC recall is listed on this page, newest first.
Why are PFIZER INC products recalled?
The most common reasons on record: Chemical contamination: emission of strong odor after package was opened. (7); CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits. (3); Chemical contamination: emission of strong odor after package was opened.. (3); Failed Dissolution Specifications (3).
What should I do if I have a recalled PFIZER INC product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new PFIZER INC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.