State

Alabama product recalls

73,809 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,378
Critical: 1,129
Severe: 1,605
Most recent: 2026-11-04

Of the 6,378 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,605 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42676–42700 of 80187

HighFDA (Devices)·Z-1180-2018·2018-04-04
BD Vacutainer Blood Collection Tubes Recalled for Residual Blood on Stopper
Becton Dickinson is recalling 1,976,000 BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tubes because increased residual blood was found on the top of the stopper well after venipuncture.
Product
BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047 Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1232-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System after a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC NAIL 125 DEG X 13MM STER TROC NAIL 130 DEG X 13MM STER TROC NAIL 135 DEG X 13MM The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1229-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System because a device performance review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System TROCH NAIL ST 11X180 125DG STRL TROCH NAIL ST 11X180 130DG STRL TROCH NAIL ST 11X180 135DG STRL The Trochanteric Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1258-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 46mm, REF 804-07-460 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1174-2018·2018-04-04
ConMed Mini Infant Radiotranslucent Electrodes Recalled for Adhesive Defect
ConMed is recalling 18,720 Mini Infant Radiotranslucent Electrodes because adhesive on contact wires may impede conductivity and cause device failure.
Product
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, REF/Catalog Number 2602 Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602 electrodes…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1181-2018·2018-04-04
Ohmeda Medical Recalls Rotating IV Poles Due to Fall Risk
Ohmeda Medical is recalling 1,179 rotating IV poles because they may fall, posing a risk of injury to patients, bystanders, or operators.
Product
Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that may be purchased to facilitate attachment and consolidation of patient equipment to one central patient care area. Devices commonly attached to IV poles…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1257-2018·2018-04-04
Encore Medical Recalls Altivate Anatomic Pegged Glenoid Trial Instruments
Encore Medical is recalling 92 units of Altivate Anatomic Pegged Glenoid Trials because the peg base design is larger on the trials than on the implants.
Product
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 42mm, REF 804-07-420 Product Usage: The AltiVate Anatomic Shoulder System is a total shoulder system indicated as an anatomic shoulder joint replacement for patients suffering from pain and dysfunction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1234-2018·2018-04-04
Zimmer Biomet Recalls ACE Trochanteric Nail System Due to Performance Failure
Zimmer Biomet is recalling the ACE Trochanteric Nail System after a Device Performance Review failed clinical analysis for survivorship.
Product
ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN LAG SCREW 65MM STERILE ATN LAG SCREW 70MM STERILE ATN LAG SCREW 75MM STERILE ATN LAG SCREW 80MM STERILE ATN LAG SCREW 85MM STERILE ATN LAG SCREW 90MM STERILE ATN LAG SCREW 95MM STERILE ATN LAG SCREW 100MM…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1185-2018·2018-04-04
Cook Inc. Recalls IVF Embryo Transfer Syringes Due to Quality Testing Gaps
Cook Inc. is recalling specific lots of Norm-Ject Tuberkulin Syringes used for IVF embryo transfer because they were distributed without completed quality testing.
Product
Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 Product Usage: Used to place in vitro fertilized (IVF) embryos into the uterine cavity. Intended for one-time use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1213-2018·2018-04-04
Konica Minolta Sonimage HS1 Ultrasound Kit AC Adapter Recall
Konica Minolta is recalling 85 Sonimage HS1 Ultrasound Kit AC adapters due to a risk of circuit board breakage and smoke emission.
Product
Sonimage HS1 Ultrasound Kit AC adapter, Product Number: A8WA, UDI: 04560141944534
Category
Medical Device
Distribution
35 states
ModerateFDA (Devices)·Z-1238-2018·2018-04-04
Zimmer Biomet Recalls Partial Knee Spacer Block Instruments
Zimmer Biomet is recalling specific Persona Partial Knee spacer block instruments because they do not fit in the alignment tower instrument or handle.
Product
Persona Partial Knee spacer block instruments; (1) 8mm block, Model Number: 42-5399-035-08; (2) 9mm block, Model Number:42-5399-035-09; (3) 10mm block, Model Number: 42-5399-035-10; (4) 12mm block, Model Number: 42-5399-035-12; (5) 14mm block, Model Number: 42-5399-035-14 A…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1269-2018·2018-04-04
Roche Modular E 170 Analyzer Recalled for Questionable Results
Roche Diagnostics is recalling Modular E 170 Analyzers because using 13 mm sample tubes without adapters may cause questionable test results.
Product
Modular E 170 Analyzer: Immunoassay Chemistry Analyzer, Chemistry (Photometric, Discrete) for clinical use, Catalog Numbers: 03739040692, 03023109001, 05023599001, 05023572001, 03739040001 & 03023109973.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1190-2018·2018-04-04
Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Mislabeled Lots
Zimmer Dental Inc is recalling Tapered Screw-Vent MTX dental implants because two lots with different thread diameters were commingled and may be mislabeled.
Product
Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSV4B10.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0612-2018·2018-04-04
Akorn Recalls 24-Hour Oral Care Kits Due to Low Chlorhexidine Levels
Akorn, Inc. is recalling 24-Hour Oral Care q2 Kits because the chlorhexidine gluconate oral rinse contained in some units had low potency levels.
Product
24-HOUR Oral Care q2 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1173-2018·2018-04-04
Biomet Recalls Orthopedic Implants Due to Screw Hole Mismatch
Biomet is recalling 634 Zimmer Biomet Comprehensive Segmental Revision System implants because a screw hole mismatch may prevent proper assembly during surgery.
Product
Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic implants for Proximal Humeral Reconstruction, Distal Humeral Reconstruction, and Total Humeral Reconstruction
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1209-2018·2018-04-04
Johnson & Johnson Recalls ACUVUE OASYS Contact Lenses Due to Foreign Matter
Johnson & Johnson Vision Care is recalling specific lots of ACUVUE OASYS contact lenses because foreign matter was found between the blister package and foil.
Product
ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1211-2018·2018-04-04
Johnson & Johnson Recalls 1-DAY ACUVUE Moist for Astigmatism Contact Lenses
Johnson & Johnson Vision Care is recalling 1-DAY ACUVUE Moist for Astigmatism contact lenses due to reports of foreign matter found between the blister package and foil.
Product
1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0611-2018·2018-04-04
Akorn Recalls Subpotent Chlorhexidine Gluconate Oral Rinse Unit Dose Cups
Akorn, Inc. is recalling Chlorhexidine Gluconate Oral Rinse unit dose cups due to product crystallization and low assay results.
Product
Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cups (NDC 50383-720-15) packaged in 100-count (10 x 10) cups per case pack (NDC 50383-720-18 or 50383-720-19), Rx Only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1241-2018·2018-04-04
Encore Medical Recalls AltiVate Reverse Humeral Socket Shell Trials
Encore Medical is recalling AltiVate Reverse Humeral Socket Shell Trials due to broken or missing screws and retaining clips.
Product
AltiVate Reverse INSTRUMENTATION, HUMERAL SOCKET SHELL TRIAL, STANDARD, REF 804-06-152, Qty: 01, Encore Medical, LP Orthopedic surgical instrument. Product Usage: The humeral socket shell trial is used to replicate/trial the shell geometry of the AltiVate Reverse Standard…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1210-2018·2018-04-04
Johnson & Johnson Recalls ACUVUE ADVANCE Contact Lenses Due to Foreign Matter
Johnson & Johnson Vision Care is recalling specific lots of ACUVUE ADVANCE contact lenses because foreign matter was found between the blister package and foil.
Product
ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1272-2018·2018-04-04
SIE AG Recalls FEMTO LDV Z8 Femtosecond Surgical Lasers
SIE AG is recalling 125 FEMTO LDV Z8 femtosecond surgical lasers worldwide due to usability and performance improvements identified after a cataract procedure complication.
Product
The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser is an ophthalmic surgical laser intended for use in the creation of corneal incisions indicated for use in patients undergoing LASIK surgery, tunnel creation for implantation of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0608-2018·2018-04-04
Paddock Recalls Evamist Estradiol Spray Due to Vial Cracks
Paddock Laboratories is recalling 52,596 bottles of Evamist (estradiol) transdermal spray because cracks in the vial neck may cause product evaporation, leaking, or dispensing failure.
Product
EVAMIST — EVAMIST (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1270-2018·2018-04-04
Roche cobas e 411 Analyzer Recall for Questionable Results
Roche Diagnostics is recalling cobas e 411 Immunoassay Analyzers because using 13 mm sample tubes without adapters may cause questionable results.
Product
cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical use), Catalog Numbers: 04775201001 (rack system), 04775279001 (disk system), 04775201973 (rack system) & 04775279973 (disk system).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1189-2018·2018-04-04
Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Labeling Error
Zimmer Dental Inc is recalling Tapered Screw-Vent MTX dental implants because two lots were inadvertently commingled during manufacturing, potentially resulting in mislabeling.
Product
Tapered Screw-Vent MTX, Dental Implant, sterile. Model TSVTB10.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1242-2018·2018-04-04
Mindray Gas Module 3 monitoring spirometer recalled for regulatory changes
Mindray DS USA is recalling 1,719 Gas Module 3 monitoring spirometers because the firm made multiple changes to the product requiring the submission of a new 510(k) premarket notification.
Product
Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device designed to monitor airway gases during anesthesia and/or assisted respiration. Monitored gases includes O2, CO2, N2O and anesthetic agents Halothane…
Category
Medical Device
Distribution
Distributed nationwide