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.

42826–42850 of 80187

HighFDA (Devices)·Z-1070-2018·2018-03-21
Stanbio Recalls RaPET RF Latex Reagent Due to False Positive Test Results
Stanbio Laboratory is recalling RaPET RF Latex Reagent because it causes all patient serum samples to yield weakly positive test results.
Product
RaPET¿ RF Latex Reagent used as a component in the following kits: RaPET RF (1155-100, Control# 173201 expiry 2019-04-30) RF Latex (1156-001, Control# 172224 expiry 2019-12-31) RF Latex (1155L-100B, Control # 172701 expiry 2019-09-30 and Control # 173262 expiry 2019-12-31)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1009-2018·2018-03-21
Zimmer Biomet Recalls Nondegradable Soft Tissue Fixation Fasteners
Zimmer Biomet is recalling 429 units of nondegradable soft tissue fixation fasteners because the implant shaft may shift and fall out during device opening.
Product
fastener, fixation, nondegradable, soft tissue
Category
Medical Device
Distribution
11 states
HighFDA (Food)·F-0929-2018·2018-03-21
Plant Devas Blue Face Care Kit Recalled for Microbial Contamination
Plant Devas Inc. is recalling the Blue Face Care Kit because FDA testing found excessive and virulent microorganisms in the product.
Product
Blue Face Care Kit; Each kit contains: Blue Lavender Cleansing Milk 1 fl oz bottle Lavender Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - BLUE 0.13 fl oz vial Blue Chamomile Day Moisturizer 0.17 fl oz jar Green Tea Clay 0.1 oz jar…
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0977-2018·2018-03-21
ZOLL Adult Defibrillator Electrodes Recall for Pediatric Energy Delivery Risk
ZOLL Medical is recalling specific adult defibrillator electrodes that may cause R Series devices to deliver pediatric energy levels instead of adult levels.
Product
OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI: 10847946016279) and 8900 0224 01 (single electrode, UDI: 00847946016272) Product Usage: Intended Use: Defibrillation, Cardioversion, Noninvasive Pacing, EGG…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0989-2018·2018-03-21
Alden Classic 55 Toric Contact Lenses Recalled for Sterility Issues
Alden Optical is recalling Alden Classic 55 Toric Daily Wear Soft contact lenses because they lack sterility assurance. The recall affects units distributed in the US and Canada.
Product
Alden Classic 55 Toric Daily Wear Soft contact; Catalog Number: AOCLT55 Product Usage: The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0968-2018·2018-03-21
BD Vacutainer K2 EDTA Blood Collection Tubes Recalled for Additive Deficiency
Becton Dickinson is recalling specific lots of BD Vacutainer K2 EDTA blood collection tubes because they may contain insufficient anticoagulant, potentially causing erroneous test results.
Product
BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 x 75 mm x 2.0 mL). Catalog Number: 367841. Used for whole blood hematology determinations, immunohematology testing and blood donor screening.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1037-2018·2018-03-21
Zimmer Biomet Recalls Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 knee implants because LDPE packaging may leave residue on the polished surface.
Product
LCCK FEM IMPLANT SZ C-L LCCK FEM IMPLANT SZ C-R LCCK FEM IMPLANT SZ D-R LCCK FEM IMPLANT SZ E-L LCCK FEM IMPLANT SZ E-R LCCK FEM IMPLANT SZ F-L LCCK FEM IMPLANT SZ F-R This device is indicated for patients with severe knee pain and disability
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1029-2018·2018-03-21
Zimmer Biomet Recalls Versus 8 Inch Beaded Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 Versus 8 Inch Beaded hip implants because LDPE packaging may leave residue on the polished surface.
Product
VERSYS 8 INCH BEADED FC 12X200MM STR STD BODY/NECK 13X200MM STR STD BODY/NECK 14X200MM STR STD BODY/NECK REV 13.5X200MM BWD LT 15X200MM STR STD BODY/NECK REV 13.5X200MM BWD RT REV 15.0X200MM BWD LT REV 15.0X200MM BWD RT REV 16.5X200MM BWD LT REV 16.5X200MM BWD RT…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1035-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
LPS OPTION FEMORAL C-L LPS OPTION FEMORAL C-R LPS OPTION FEMORAL D-L LPS OPTION FEMORAL D-R LPS OPTION FEMORAL E-L LPS OPTION FEMORAL E-R LPS OPTION FEMORAL F-L LPS OPTION FEMORAL F-R LPS OPTION FEMORAL G-L LPS OPTION FEMORAL G-R LPS OPTION FEMORAL H-L This device…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1055-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE bag packaging may leave residue on the polished surfaces.
Product
FEM PRC LT M/RT L SML FEM PRC RT M/LT L SML FEM PRC LT M/RT L SML+ FEM PRC RT M/LT L SML+ FEM PRC LT M/RT L REG FEM PRC RT M/LT L REG FEM PRC LT M/RT L REG+ FEM PRC RT M/LT L REG+ FEM PRC LT M/RT L LGE…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1060-2018·2018-03-21
Zimmer Biomet Recalls Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 Natural-Knee Flex System femoral components because LDPE packaging may leave residue on the polished implant surface.
Product
GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM GENDER SOLUTIONS FEMALE (GSF) FEMORAL COMPONENT NONPOROUS¿ N-K FLX GSF NP FEM SZ 0 RT N-K FLX GSF NP FEM SZ 4 LT N-K FLX GSF NP FEM SZ 4 RT Components with CSTi porous coating are indicated for uncemented or cemented use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1030-2018·2018-03-21
Zimmer Biomet Recalls Knee Prostheses Due to Packaging Residue
Zimmer Biomet is recalling specific knee prostheses because the packaging bags may leave residue on the implant surface.
Product
CR POR FEM HATCP SIZE E/L SIZE F/L Knee Prosthesis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0935-2018·2018-03-21
Becton Dickinson Recalls Mislabeled Difco Agar Noble Laboratory Product
Becton Dickinson & Co. is recalling 216 bottles of Difco Agar Noble because the product was mislabeled and inadvertently sold as Noble Agar.
Product
Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in electrophoretic and nutritional procedures and in preparing microbiological culture media when increased purity is required.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1033-2018·2018-03-21
Zimmer Biomet Recalls Natural-Knee II Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 Natural-Knee II knee implants because LDPE packaging may leave residue on the polished implant surfaces.
Product
NP FEM LT SZ0 NATURAL-KNE NP FEM RT SZ0 NATURAL-KNE NP FEM LT SZ2 NATURAL-KNE NP FEM RT SZ2 NATURAL-KNE NP FEM LT SZ3 NATURAL-KNE The Natural-Knee II System with Cancellous-Structured Titanium (CSTi) Porous Coating
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1023-2018·2018-03-21
Zimmer Biomet Recalls Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling specific Versus hip prostheses because LDPE packaging may leave residue on the polished implant surface.
Product
VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1018-2018·2018-03-21
Zimmer Biomet Recalls Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip implants because LDPE packaging may leave residue on the polished surface.
Product
CPT 12/14 COCR SIZE 2 EXT prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1019-2018·2018-03-21
Zimmer Biomet Recalls Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip implants because LDPE packaging may leave residue on the polished surface.
Product
CPT 12/14 COCR SIZE 2 STD prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1038-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling specific hip and knee implants because the packaging bags may leave residue on the polished surfaces.
Product
LPS POROUS FEM IMPLANT SZ G-L LPS PRECOAT FEM IMPLANT SZ G-L This device is indicated for patients with severe knee pain and disability
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1031-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surface.
Product
CR-FLX POR HATCP FEM C-L MINUS CR-FLX POR HATCP FEM C-R MINUS CR-FLX POR HATCP FEM D-L MINUS CR-FLX POR HATCP FEM D-R MINUS CR-FLX POR HATCP FEM E-L MINUS CR-FLX POR HATCP FEM E-R MINUS CR-FLX POR HATCP FEM F-L MINUS CR-FLX POR HATCP FEM F-R MINUS CR-FLX POR HATCP FEM…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1043-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-R LPS-FLEX OPTION FEMORAL D-L LPS-FLEX OPTION FEMORAL D-R LPS-FLEX OPTION FEMORAL E-L LPS-FLEX OPTION FEMORAL E-R LPS-FLEX OPTION FEMORAL F-L LPS-FLEX OPTION FEMORAL F-R LPS-FLEX OPTION…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0592-2018·2018-03-21
American Pharmaceutical Ingredients Recalls Sermorelin Acetate Powder Due to Stability Data
American Pharmaceutical Ingredients LLC is recalling Sermorelin Acetate powder because stability data does not support the listed expiration dates.
Product
Sermorelin Acetate, powder, a) 1 GM-bottle (NDC58597-8092-1) b) 5 GM-bottle (NDC 58597-8092-2) c) 10 GM-bottle (NDC 58597-8092-4) API American Pharmaceutical Ingredients
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1050-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE bag packaging may leave residue on the polished surfaces.
Product
CR-FLEX PCT FEM B-R CR-FLEX PCT FEM C-L CR-FLEX PCT FEM C-R CR-FLEX PCT FEM D-L CR-FLEX PCT FEM D-R CR-FLEX PCT FEM E-L CR-FLEX PCT FEM E-R CR-FLEX PCT FEM F-L CR-FLEX PCT FEM F-R CR-FLEX PCT FEM G-L CR-FLEX PCT FEM G-R This device is indicated for patients with…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1041-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
CR PRECOAT FEM COMP SIZE BMR CR PRECOAT FEM COMP SIZE C/R CR PRECOAT FEM COMP SIZE D/R CR PRECOAT FEM COMP SIZE E/R CR PRECOAT FEM COMP SIZE F/R CR PRECOAT FEM COMP SIZE G/L CR PRECOAT FEM COMP SIZE H/L CR PRECOAT FEM COMP SIZE H/R CR POROUS FEM COMP SIZE E/L CR POROUS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1059-2018·2018-03-21
Zimmer Biomet Recalls Hip and Knee Implants Due to Packaging Residue
Zimmer Biomet is recalling 13,227 hip and knee implants because LDPE packaging may leave residue on the polished surfaces.
Product
CR-FLEX GSF PRECOAT SZ C-L¿ CR-FLEX GSF PRECOAT SZ C-R¿ CR-FLEX GSF PRECOAT SZ D-L¿ CR-FLEX GSF PRECOAT SZ D-R¿ CR-FLEX GSF PRECOAT SZ E-L¿ CR-FLEX GSF PRECOAT SZ E-R¿ CR-FLEX GSF PRECOAT SZ F-L¿ CR-FLEX GSF PRECOAT SZ F-R¿ CR-FLEX GSF PRECOAT SZ G-L¿ CR-FLEX GSK…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1015-2018·2018-03-21
Zimmer Biomet Recalls Hip Implants Due to Packaging Residue
Zimmer Biomet is recalling specific hip implants because LDPE packaging may leave residue on the polished surface.
Product
CPT 12/14 COCR REVISION SIZE 2 180MM prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Category
Medical Device
Distribution
Distributed nationwide